ObesityE-FLIPNCT01820338
Extension Family Lifestyle Intervention Project (E-FLIP for Kids)
A study testing Behavioral Child Tx Contacts, Behavioral Parent-Tx Contacts and Dietary and Physical Activity Information in people with Obesity, run by University of Florida at 1 site in United States.
Trial summary
The Extension Family Lifestyle Intervention Project (E-FLIP for Kids) trial will evaluate the impact of a community based intervention delivered to families in rural settings utilizing the existing Cooperative Extension Service network on child dietary intake and weight. Read more about this study
- Who is it for?
- Ages 8 to 12 years
- Conditions the study is for
- Obesity
- What is being tested?
- Behavioral Child Tx Contacts, Behavioral Parent-Tx Contacts and Dietary and Physical Activity Information
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 314 participants
- Where
- 1 siteUnited States
- Study dates
- Jul 2009to Apr 2014
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 8 to 12 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Children between the ages of 8 and 12 years,
- BMI equal to or above the 85th percentile for age and gender
- Child and participating parent(s) or legal guardian(s) are required to live within the same dwelling in a rural county.
- Participating parents or legal guardians must be age 75 years or less.
Who cannot join
- Child or participating parent has a dietary or exercise restriction
- Medical condition that contraindicates mild energy restriction or moderate physical activity
- Children or adults cannot be engaged in another weight control program.
- Unwilling or unable to give informed consent,
- Parent(s) or legal guardian(s) unable to read English at approximately the 5th grade level,
- Unwilling to accept random assignment,
- Unable to travel to the Extension office for intervention sessions,
- Likely to move out of the county within the next 24 months.
Trial locations and contacts
1 site in 1 country.
About this study
The Extension Family Lifestyle Intervention Project (E-FLIP for Kids) trial will evaluate the impact of a community based intervention delivered to families in rural settings utilizing the existing Cooperative Extension Service network on child dietary intake and weight. Specifically, the E-FLIP for Kids study will determine if behavioral treatments for child obesity lead to greater improvement in child weight compared to educational only treatment.Participants will include 240 parent-child dyads from ten rural counties in north central Florida. Study outcomes will be measure prior to treatment, at the end of treatment (month 12) and at one year follow-up (month 24). All treatment meetings will be held at Cooperative Extension Service offices within each participating county.
Read the detailed description
The study sample will include 240 overweight and obese children, ages 8 to 12 years, and their parent(s) from rural counties in North Central Florida. Participants will be randomized to one of three conditions: family-based (FB) healthy lifestyle intervention, parent-only (PO) healthy lifestyle intervention, and health education control (HEC) condition. Each of the treatment conditions will involve 23 group meetings delivered on the same schedule.
Recruitment will include direct solicitation methods combined with culturally-tailored efforts targeting the recruitment of minority participants. Direct solicitation methods will entail direct mailings to households and to health-care providers, a press release, and presentations/brochure distribution by Extension agents and research team members at churches, social organizations, community events, and through local businesses. Brochures will also be distributed through local schools. Recruitment information will contain a toll-free phone number to our research office. Potential participants will be encouraged to call our office to learn more about the study and complete an initial phone screen. The phone calls will be received by trained staff that will describe the study and perform a brief phone screen in order to determine initial eligibility. Those families who meet initial eligibility and express interest will be scheduled for an in-person screening visit to determine their final eligibility for the program.
Participants (child and parent) will complete assessment measures at an initial screening visit, pre-start baseline assessment, post-treatment assessment (12 months after the baseline assessment), and a follow-up assessment (24 months after the baseline assessment).
At the initial in-person screening visit interested participants (child and parent/legal guardian) will complete informed consent procedures and then measures of height and weight, medical history questionnaires, and a general family information form. Parents will complete questionnaires regarding family functioning, parent psychological functioning, parent mobility, child behavior, reasons for seeking treatment, and family cost of program participation. Children will complete questionnaires regarding reasons for joining the program and social interactions. In addition, the child will be assessed for resting heart rate and blood pressure.
The pre-start/baseline assessment visit will occur approximately one to two weeks prior to the beginning of the intervention. At this assessment children and parents will be measured for height and weight, and the child's waist circumference will also be assessed. Families will complete a packet of self-report study questionnaires. Children will be assessed for blood pressure and heart rate. Children's body fat percentage will be assessed by an electrical impedence scale. Child will be asked to wear an armband accelerometer for seven days following the assessment. Children will also be asked to complete one finger prick (with collection of approximately 2-3 drops of blood) to assess blood lipids and HbA1C using a point-of-care device. A 20 meter shuttle physical fitness assessment will also be completed by children to assess their level of physical fitness. The finger prick, blood pressure, physical fitness, and heart rate assessment protocol will be completed by study medical personnel trained in these procedures. Children, with help from their parents, will complete measures of the child's dietary intake and physical activity habits, eating behaviors, qualify of life, body image, and pubertal development. Parents will complete measures about their own dietary intake and physical activity habits, the family feeding environment, perceive family support and social problem solving abilities. At the end of this baseline assessment visit, participants will be notified as to which of the three treatment conditions they were randomized.
The same assessment protocol administered at the baseline visit will be administered at the post-treatment assessment, and follow-up assessment. Measures of post-treatment satisfaction will also be administered to the child and parent at these two follow-up assessments.
Family-Based Group Intervention Condition: Each parent and child dyad will participate in 23 group meetings. Children and parents will meet in simultaneous, but separate, parent and child groups at each meeting. The intervention will include weekly sessions for the first 8 weeks and biweekly sessions for the next 8 weeks. Families will also participate in a maintenance intervention for the next eight months (months 5 to 12) that includes one session per month, with the exception of month 8, which will include 4 weekly sessions. For all child and parent participants, the primary treatment objectives will be to decrease caloric intake in a nutritionally sound manner and to increase moderate intensity exercise. Changes in dietary habits will be addressed via a modified version of the Stoplight System. The stoplight system is designed to teach children and parents to classify foods according to the colors of the stoplight. Green foods are "go foods", are foods high in nutrients and low in calories (i.e., fruits and vegetables). Yellow foods are "caution" foods. Yellow foods have lots of nutrition, but also significant calories and should be eaten in moderation. Red foods are "stop" foods. These foods are high in calories relative to nutrients. Red foods should be limited, but are not considered forbidden. Weekly goals will target gradual reductions in caloric intake through limiting consumption of high-fat/high-sugar foods "Red foods" and increasing consumption of fruits and vegetables. Children and adults will be encouraged to eat a well-balanced diet based on the food guide pyramid. Parents and children will also be given pedometers (step counters) and they will be asked to keep track of the number of steps they take each day. Each week parents and children will set goals to gradually increase the number of steps they take each day. Parent and their children will be asked to record what they eat and drink, as well as their physical activity (number of steps taken) on daily food logs.
Parent Group Session. Each session will last 90 minutes and will include three segments. In the first segment will review parent and child progress in implementing the strategies recommended and goals set for changing their eating or exercise in the previous session. Parents will discuss with group leaders the successes, challenges, and barriers encountered as they attempted to make lifestyle changes over the past week, as well as discuss possible strategies for overcoming various challenges. The second segment will focus on the specific "topic of the day" or "session lesson". The third segment will involve bringing the children and parents back together at the end of each session to set specific goals for the next week.
Child Group Session. Each session will last 90 minutes. During the first part of the session we will review the children's progress in achieving their dietary and physical activity goals over the previous week. After a private weigh-in, child participants will describe the progress they achieved in reaching their dietary and physical activity goals. Good progress will be highlighted by strong positive feedback. The second segment will include an exercise or game component to demonstrate strategies/activities to help children keep physically active including activities such as Frisbee, flashlight tag, watermelon relay, jump rope, kickball and dancing. Third, the children and group leaders will prepare and sample a variety of healthy snacks including fruits and vegetables with various healthy low fat dips, bagels with low fat cream cheese, low fat cheese quesadillas, fruit smoothies, and yogurt fruit parfaits. During the food sampling portion of each session, fun and educational activities will be used to teach children about nutrition (e.g., recognizing calorie and fat content of foods via "signals" of the Stoplight program), strategies to increase physical activity, behavioral management skills (self-monitoring and goal setting), and strategies to cope with psychosocial concerns (i.e., building self-esteem) and how to also support their parents.
Parent-only Group Intervention Condition: Only the participating parent(s) will attend 23 group meetings over the course of one year. The parent-only interventions will meet on the same schedule as the family-based intervention. The intervention will include weekly sessions for the first 8 weeks and biweekly sessions for the next 8 weeks. Families will also participate in a maintenance intervention for eight months (months 5 to 12) that includes one session per month, with the exception of month 8, which will include 4 weekly sessions.
Each session will last 90 minutes and will include three segments, similar to the parent group previously described in the FB intervention. The sessions for parents in the parent-only program will be structured the same as the parents sessions for the family-based intervention (described above) and will also cover the same topics. As with the family-based intervention, the parent and their children assigned to the parent-only intervention will be asked to record what they eat and drink, as well as their physical activity, on a daily basis. As children will not be attending group sessions in this condition, an emphasis will be placed on helping parents effectively communicate the topics of each session to the target child at home, as well as teaching parents how to work with their children to set goals together and monitor their food intake and physical activity. Each week group interventionists will model the goal setting process with parents and suggest a general range of age-appropriate dietary and physical activity targets that might be appropriate for each child and parent.
Health Education Condition: Both the child and parent will attend the treatment sessions in this program. This condition will include 23 group meetings on the same schedule as the previously described conditions. Each session will last 90 minutes. The Health Education condition will be tailored for children and families, and will include a series of meetings addressing key aspects of nutrition, physical activity, and health promotion. The health education curriculum will include topics such as national guidelines regarding proper nutrition, guidelines for physical activity, strategies to cope with stress, healthy sources and guidelines for intake of fiber, calcium, protein, grains \& carbohydrates. Topics will also include use of vitamin \& mineral supplements, dental and sleep hygiene, self-esteem, family communication, and assertiveness training in dealing with peer victimization. The families in the Health Education group will not receive training in behavioral self-regulation strategies, such as goal setting and self-monitoring. Children will participate in a group physical activity during each session such as frisbee, jump rope, stoplight tag. They will also sample healthy snacks such as pretzels or fruits and vegetables. There will be no discussion of implementing these activities and preparing healthy snacks in other settings. Children will not help prepare the snack items.
- Conditions
- Obesity
- Being tested
- Behavioral Child Tx Contacts, Behavioral Parent-Tx Contacts, Dietary and Physical Activity Information
- Keywords
- Children, Obesity, Intervention
- Medical subject headings
- Obesity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Behavioral Child Tx ContactsBehavioural
Each parent and child dyad will participate in group meetings. Children and parents will meet in simultaneous, but separate, groups at each meeting. The intervention will include 12 sessions over 16 weeks. Families will also participate in a maintenance intervention for the next eight months. The primary treatment objectives will be to decrease caloric intake in a nutritionally sound manner and to increase moderate intensity exercise. Changes in dietary habits will be addressed via a modified version of the Stoplight System. Children and adults will be encouraged to eat a well-balanced diet based on the food guide pyramid. Parents and children will also be given pedometers and they will be asked to keep track of the number of steps they take each day. Each week parents and children will set goals to gradually increase physical activity. Parent and their children will be asked to record what they eat and drink, as well as their physical activity on daily food logs.
Behavioral Parent-Tx ContactsBehavioural
Only the participating parent(s) will attend group meetings. The intervention will include weekly sessions for the first 8 weeks and biweekly sessions for the next 8 weeks. They will also participate in a maintenance intervention for eight months. Each session will last 90 minutes. The sessions for parents in the parent-only program will be structured the same as the parents sessions for the family-based intervention and will also cover the same topics. As with the family-based intervention, the parent and their children assigned to the parent-only intervention will be asked to record what they eat and drink, as well as their physical activity, on a daily basis. Each week group interventionists will model the goal setting process with parents and suggest a general range of age-appropriate dietary and physical activity targets that might be appropriate for each child and parent.
Dietary and Physical Activity InformationOther
Both the child and parent will attend the treatment sessions in this program. The condition will include a series of meetings addressing key aspects of nutrition, physical activity, and health promotion such as national guidelines regarding proper nutrition, guidelines for physical activity, strategies to cope with stress, healthy sources and guidelines for intake of fiber, calcium, protein, grains \& carbohydrates. Topics will also include use of vitamin \& mineral supplements, dental and sleep hygiene, self-esteem, family communication, and assertiveness training in dealing with peer victimization. The families in the Health Education group will not receive training in behavioral self-regulation strategies, such as goal setting and self-monitoring. Children will participate in a group physical activity during each session such as frisbee, jump rope, stoplight tag. They will also sample healthy snacks such as pretzels or fruits and vegetables.
| Study group | Role | What they receive |
|---|---|---|
| Behavioral Family Intervention | Experimental | Child and Parent attend intervention including nutrition and physical activity education, plus behavioral strategies to facilitate behavior and weight status change Receives: Behavioral: Behavioral Child Tx Contacts; Behavioral: Behavioral Parent-Tx Contacts; Other: Dietary and Physical Activity Information |
| Behavioral Parent-Only Intervention | Experimental | Only parents attend intervention including nutrition and physical activity education, plus behavioral strategies to facilitate behavior and weight status change Receives: Behavioral: Behavioral Parent-Tx Contacts; Other: Dietary and Physical Activity Information |
| Education Control | Active comparator | Child and parent attend intervention that includes only nutrition and physical activity education; no instruction or assistance in the use of behavioral strategies are included in this condition Receives: Other: Dietary and Physical Activity Information |
What is being measured
The primary outcome is the main question the study is designed to answer.
Child BMI Z score
Change in Child BMI Z score from baseline to year 2
Measured: 2 years
Secondary outcomes (2)
Child caloric intake
Change in child caloric intake from baseline to year 2.
Measured: 2 years
Child Physical Activity
Change in physical activity from baseline to year 2
Measured: 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Mar 2013 (estimated)
- Study startJul 2009
- Primary completionApr 2014
- Study completionApr 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (8)Papers the sponsor has linked to this study.
- Other trials for ObesityStudies of the same condition, open and under way.
- More trials run by University of FloridaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 314 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Florida
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- David M Janicke, Ph.D., Principal investigator, University of Florida
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01820338
- Sponsor's protocol ID
- 204-2009
- Acronym
- E-FLIP
- Status last verified
- Mar 2015
- First submitted
- 19 Mar 2013
- Last updated
- 20 Mar 2015
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Janicke DM, Lim CS, Perri MG, Bobroff LB, Mathews AE, Brumback BA, Dumont-Driscoll M, Silverstein JH. The Extension Family Lifestyle Intervention Project (E-FLIP for Kids): design and methods. Contemp Clin Trials. 2011 Jan;32(1):50-8. doi: 10.1016/j.cct.2010.08.002. Epub 2010 Aug 11.
PubMed 20708715Lim CS, Mayer-Brown SJ, Clifford LM, Janicke DM. Pain is Associated with Physical Activity and Health-Related Quality of Life in Overweight and Obese Children. Child Health Care. 2014 Jul;43(3):186-202. doi: 10.1080/02739615.2013.837825.
PubMed 25484483Lim, C.S. & Janicke, D.M. (2013). Barriers related to delivering pediatric weight management interventions to children and families from rural communities. Children's Health Care, 42, 214-230.
Gowey MA, Lim CS, Clifford LM, Janicke DM. Disordered eating and health-related quality of life in overweight and obese children. J Pediatr Psychol. 2014 Jun;39(5):552-61. doi: 10.1093/jpepsy/jsu012. Epub 2014 Mar 26.
PubMed 24676798Fedele DA, Janicke DM, Lim CS, Abu-Hasan M. An examination of comorbid asthma and obesity: assessing differences in physical activity, sleep duration, health-related quality of life and parental distress. J Asthma. 2014 Apr;51(3):275-81. doi: 10.3109/02770903.2013.873807. Epub 2014 Jan 10.
PubMed 24320738Labyak CA, Janicke DM, Lim CS, Colee J, Mathews AE. Anthropometrics to Identify Overweight Children at Most Risk for the Development of Cardiometabolic Disease. Infant Child Adolesc Nutr. 2013 Dec;5(6):341-346. doi: 10.1177/1941406413501379.
PubMed 25485038Janicke DM, Lim CS, Perri MG, Mathews AE, Bobroff LB, Gurka MJ, Parish A, Brumback BA, Dumont-Driscoll M, Silverstein JH. Featured Article: Behavior Interventions Addressing Obesity in Rural Settings: The E-FLIP for Kids Trial. J Pediatr Psychol. 2019 Sep 1;44(8):889-901. doi: 10.1093/jpepsy/jsz029.
PubMed 31039250Graef DM, Janicke DM, McCrae CS. Sleep patterns of a primarily obese sample of treatment-seeking children. J Clin Sleep Med. 2014 Oct 15;10(10):1111-7. doi: 10.5664/jcsm.4112.
PubMed 25317092
Study at a glance
From the registry record, last updated by the sponsor on 20 Mar 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Extension Family Lifestyle Intervention Project (E-FLIP for Kids)
- ClinicalTrials.gov ID
- NCT01820338
- Acronym / sponsor ID
- E-FLIP / 204-2009
- Conditions
- Obesity
- Keywords
- Children, Obesity, Intervention
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 314 participants (actual)
- Lead sponsor
- University of FloridaUniversity, hospital or other
- Study start
- Jul 2009
- Primary completion
- Apr 2014 (actual)
- Study completion
- Apr 2014 (actual)
- First posted
- 28 Mar 2013 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The Extension Family Lifestyle Intervention Project (E-FLIP for Kids) trial will evaluate the impact of a community based intervention delivered to families in rural settings utilizing the existing Cooperative Extension Service network on child dietary intake and weight. Specifically, the E-FLIP for Kids study will determine if behavioral treatments for child obesity lead to greater improvement in child weight compared to educational only treatment.Participants will include 240 parent-child dyads from ten rural counties in north central Florida. Study outcomes will be measure prior to treatment, at the end of treatment (month 12) and at one year follow-up (month 24). All treatment meetings will be held at Cooperative Extension Service offices within each participating county.
Detailed description
The study sample will include 240 overweight and obese children, ages 8 to 12 years, and their parent(s) from rural counties in North Central Florida. Participants will be randomized to one of three conditions: family-based (FB) healthy lifestyle intervention, parent-only (PO) healthy lifestyle intervention, and health education control (HEC) condition. Each of the treatment conditions will involve 23 group meetings delivered on the same schedule.
Recruitment will include direct solicitation methods combined with culturally-tailored efforts targeting the recruitment of minority participants. Direct solicitation methods will entail direct mailings to households and to health-care providers, a press release, and presentations/brochure distribution by Extension agents and research team members at churches, social organizations, community events, and through local businesses. Brochures will also be distributed through local schools. Recruitment information will contain a toll-free phone number to our research office. Potential participants will be encouraged to call our office to learn more about the study and complete an initial phone screen. The phone calls will be received by trained staff that will describe the study and perform a brief phone screen in order to determine initial eligibility. Those families who meet initial eligibility and express interest will be scheduled for an in-person screening visit to determine their final eligibility for the program.
Participants (child and parent) will complete assessment measures at an initial screening visit, pre-start baseline assessment, post-treatment assessment (12 months after the baseline assessment), and a follow-up assessment (24 months after the baseline assessment).
At the initial in-person screening visit interested participants (child and parent/legal guardian) will complete informed consent procedures and then measures of height and weight, medical history questionnaires, and a general family information form. Parents will complete questionnaires regarding family functioning, parent psychological functioning, parent mobility, child behavior, reasons for seeking treatment, and family cost of program participation. Children will complete questionnaires regarding reasons for joining the program and social interactions. In addition, the child will be assessed for resting heart rate and blood pressure.
The pre-start/baseline assessment visit will occur approximately one to two weeks prior to the beginning of the intervention. At this assessment children and parents will be measured for height and weight, and the child's waist circumference will also be assessed. Families will complete a packet of self-report study questionnaires. Children will be assessed for blood pressure and heart rate. Children's body fat percentage will be assessed by an electrical impedence scale. Child will be asked to wear an armband accelerometer for seven days following the assessment. Children will also be asked to complete one finger prick (with collection of approximately 2-3 drops of blood) to assess blood lipids and HbA1C using a point-of-care device. A 20 meter shuttle physical fitness assessment will also be completed by children to assess their level of physical fitness. The finger prick, blood pressure, physical fitness, and heart rate assessment protocol will be completed by study medical personnel trained in these procedures. Children, with help from their parents, will complete measures of the child's dietary intake and physical activity habits, eating behaviors, qualify of life, body image, and pubertal development. Parents will complete measures about their own dietary intake and physical activity habits, the family feeding environment, perceive family support and social problem solving abilities. At the end of this baseline assessment visit, participants will be notified as to which of the three treatment conditions they were randomized.
The same assessment protocol administered at the baseline visit will be administered at the post-treatment assessment, and follow-up assessment. Measures of post-treatment satisfaction will also be administered to the child and parent at these two follow-up assessments.
Family-Based Group Intervention Condition: Each parent and child dyad will participate in 23 group meetings. Children and parents will meet in simultaneous, but separate, parent and child groups at each meeting. The intervention will include weekly sessions for the first 8 weeks and biweekly sessions for the next 8 weeks. Families will also participate in a maintenance intervention for the next eight months (months 5 to 12) that includes one session per month, with the exception of month 8, which will include 4 weekly sessions. For all child and parent participants, the primary treatment objectives will be to decrease caloric intake in a nutritionally sound manner and to increase moderate intensity exercise. Changes in dietary habits will be addressed via a modified version of the Stoplight System. The stoplight system is designed to teach children and parents to classify foods according to the colors of the stoplight. Green foods are "go foods", are foods high in nutrients and low in calories (i.e., fruits and vegetables). Yellow foods are "caution" foods. Yellow foods have lots of nutrition, but also significant calories and should be eaten in moderation. Red foods are "stop" foods. These foods are high in calories relative to nutrients. Red foods should be limited, but are not considered forbidden. Weekly goals will target gradual reductions in caloric intake through limiting consumption of high-fat/high-sugar foods "Red foods" and increasing consumption of fruits and vegetables. Children and adults will be encouraged to eat a well-balanced diet based on the food guide pyramid. Parents and children will also be given pedometers (step counters) and they will be asked to keep track of the number of steps they take each day. Each week parents and children will set goals to gradually increase the number of steps they take each day. Parent and their children will be asked to record what they eat and drink, as well as their physical activity (number of steps taken) on daily food logs.
Parent Group Session. Each session will last 90 minutes and will include three segments. In the first segment will review parent and child progress in implementing the strategies recommended and goals set for changing their eating or exercise in the previous session. Parents will discuss with group leaders the successes, challenges, and barriers encountered as they attempted to make lifestyle changes over the past week, as well as discuss possible strategies for overcoming various challenges. The second segment will focus on the specific "topic of the day" or "session lesson". The third segment will involve bringing the children and parents back together at the end of each session to set specific goals for the next week.
Child Group Session. Each session will last 90 minutes. During the first part of the session we will review the children's progress in achieving their dietary and physical activity goals over the previous week. After a private weigh-in, child participants will describe the progress they achieved in reaching their dietary and physical activity goals. Good progress will be highlighted by strong positive feedback. The second segment will include an exercise or game component to demonstrate strategies/activities to help children keep physically active including activities such as Frisbee, flashlight tag, watermelon relay, jump rope, kickball and dancing. Third, the children and group leaders will prepare and sample a variety of healthy snacks including fruits and vegetables with various healthy low fat dips, bagels with low fat cream cheese, low fat cheese quesadillas, fruit smoothies, and yogurt fruit parfaits. During the food sampling portion of each session, fun and educational activities will be used to teach children about nutrition (e.g., recognizing calorie and fat content of foods via "signals" of the Stoplight program), strategies to increase physical activity, behavioral management skills (self-monitoring and goal setting), and strategies to cope with psychosocial concerns (i.e., building self-esteem) and how to also support their parents.
Parent-only Group Intervention Condition: Only the participating parent(s) will attend 23 group meetings over the course of one year. The parent-only interventions will meet on the same schedule as the family-based intervention. The intervention will include weekly sessions for the first 8 weeks and biweekly sessions for the next 8 weeks. Families will also participate in a maintenance intervention for eight months (months 5 to 12) that includes one session per month, with the exception of month 8, which will include 4 weekly sessions.
Each session will last 90 minutes and will include three segments, similar to the parent group previously described in the FB intervention. The sessions for parents in the parent-only program will be structured the same as the parents sessions for the family-based intervention (described above) and will also cover the same topics. As with the family-based intervention, the parent and their children assigned to the parent-only intervention will be asked to record what they eat and drink, as well as their physical activity, on a daily basis. As children will not be attending group sessions in this condition, an emphasis will be placed on helping parents effectively communicate the topics of each session to the target child at home, as well as teaching parents how to work with their children to set goals together and monitor their food intake and physical activity. Each week group interventionists will model the goal setting process with parents and suggest a general range of age-appropriate dietary and physical activity targets that might be appropriate for each child and parent.
Health Education Condition: Both the child and parent will attend the treatment sessions in this program. This condition will include 23 group meetings on the same schedule as the previously described conditions. Each session will last 90 minutes. The Health Education condition will be tailored for children and families, and will include a series of meetings addressing key aspects of nutrition, physical activity, and health promotion. The health education curriculum will include topics such as national guidelines regarding proper nutrition, guidelines for physical activity, strategies to cope with stress, healthy sources and guidelines for intake of fiber, calcium, protein, grains \& carbohydrates. Topics will also include use of vitamin \& mineral supplements, dental and sleep hygiene, self-esteem, family communication, and assertiveness training in dealing with peer victimization. The families in the Health Education group will not receive training in behavioral self-regulation strategies, such as goal setting and self-monitoring. Children will participate in a group physical activity during each session such as frisbee, jump rope, stoplight tag. They will also sample healthy snacks such as pretzels or fruits and vegetables. There will be no discussion of implementing these activities and preparing healthy snacks in other settings. Children will not help prepare the snack items.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Behavioral Family Intervention | Experimental | Behavioral: Behavioral Child Tx Contacts, Behavioral: Behavioral Parent-Tx Contacts, Other: Dietary and Physical Activity InformationChild and Parent attend intervention including nutrition and physical activity education, plus behavioral strategies to facilitate behavior and weight status change |
| Behavioral Parent-Only Intervention | Experimental | Behavioral: Behavioral Parent-Tx Contacts, Other: Dietary and Physical Activity InformationOnly parents attend intervention including nutrition and physical activity education, plus behavioral strategies to facilitate behavior and weight status change |
| Education Control | Active comparator | Other: Dietary and Physical Activity InformationChild and parent attend intervention that includes only nutrition and physical activity education; no instruction or assistance in the use of behavioral strategies are included in this condition |
Who may qualify
- Ages
- 8 to 12 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (4 listed)
- Children between the ages of 8 and 12 years,
- BMI equal to or above the 85th percentile for age and gender
- Child and participating parent(s) or legal guardian(s) are required to live within the same dwelling in a rural county.
- Participating parents or legal guardians must be age 75 years or less.
Key exclusion criteria (8 listed)
- Child or participating parent has a dietary or exercise restriction
- Medical condition that contraindicates mild energy restriction or moderate physical activity
- Children or adults cannot be engaged in another weight control program.
- Unwilling or unable to give informed consent,
- Parent(s) or legal guardian(s) unable to read English at approximately the 5th grade level,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Behavioral Child Tx ContactsEach parent and child dyad will participate in group meetings. Children and parents will meet in simultaneous, but separate, groups at each meeting. The intervention will include 12 sessions over 16 weeks. Families will also participate in a maintenance intervention for the next eight months. The primary treatment objectives will be to decrease caloric intake in a nutritionally sound manner and to increase moderate intensity exercise. Changes in dietary habits will be addressed via a modified version of the Stoplight System. Children and adults will be encouraged to eat a well-balanced diet based on the food guide pyramid. Parents and children will also be given pedometers and they will be asked to keep track of the number of steps they take each day. Each week parents and children will set goals to gradually increase physical activity. Parent and their children will be asked to record what they eat and drink, as well as their physical activity on daily food logs. | Behavioural | Behavioral Family Intervention |
| Behavioral Parent-Tx ContactsOnly the participating parent(s) will attend group meetings. The intervention will include weekly sessions for the first 8 weeks and biweekly sessions for the next 8 weeks. They will also participate in a maintenance intervention for eight months. Each session will last 90 minutes. The sessions for parents in the parent-only program will be structured the same as the parents sessions for the family-based intervention and will also cover the same topics. As with the family-based intervention, the parent and their children assigned to the parent-only intervention will be asked to record what they eat and drink, as well as their physical activity, on a daily basis. Each week group interventionists will model the goal setting process with parents and suggest a general range of age-appropriate dietary and physical activity targets that might be appropriate for each child and parent. | Behavioural | Behavioral Family Intervention, Behavioral Parent-Only Intervention |
| Dietary and Physical Activity InformationBoth the child and parent will attend the treatment sessions in this program. The condition will include a series of meetings addressing key aspects of nutrition, physical activity, and health promotion such as national guidelines regarding proper nutrition, guidelines for physical activity, strategies to cope with stress, healthy sources and guidelines for intake of fiber, calcium, protein, grains \& carbohydrates. Topics will also include use of vitamin \& mineral supplements, dental and sleep hygiene, self-esteem, family communication, and assertiveness training in dealing with peer victimization. The families in the Health Education group will not receive training in behavioral self-regulation strategies, such as goal setting and self-monitoring. Children will participate in a group physical activity during each session such as frisbee, jump rope, stoplight tag. They will also sample healthy snacks such as pretzels or fruits and vegetables. | Other | Behavioral Family Intervention, Behavioral Parent-Only Intervention, Education Control |
Primary outcome
Child BMI Z score
Time frame: 2 years
Change in Child BMI Z score from baseline to year 2
2 secondary outcomes
Child caloric intake
Time frame: 2 years
Child Physical Activity
Time frame: 2 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Mar 2015.
- Background: PubMed 20708715Janicke DM, Lim CS, Perri MG, Bobroff LB, Mathews AE, Brumback BA, Dumont-Driscoll M, Silverstein JH. The Extension Family Lifestyle Intervention Project (E-FLIP for Kids): design and methods. Contemp Clin Trials. 2011 Jan;32(1):50-8. doi: 10.1016/j.cct.2010.08.002. Epub 2010 Aug 11.
- Background: PubMed 25484483Lim CS, Mayer-Brown SJ, Clifford LM, Janicke DM. Pain is Associated with Physical Activity and Health-Related Quality of Life in Overweight and Obese Children. Child Health Care. 2014 Jul;43(3):186-202. doi: 10.1080/02739615.2013.837825.
- BackgroundLim, C.S. & Janicke, D.M. (2013). Barriers related to delivering pediatric weight management interventions to children and families from rural communities. Children's Health Care, 42, 214-230.
- Results publication: PubMed 24676798Gowey MA, Lim CS, Clifford LM, Janicke DM. Disordered eating and health-related quality of life in overweight and obese children. J Pediatr Psychol. 2014 Jun;39(5):552-61. doi: 10.1093/jpepsy/jsu012. Epub 2014 Mar 26.
- Results publication: PubMed 24320738Fedele DA, Janicke DM, Lim CS, Abu-Hasan M. An examination of comorbid asthma and obesity: assessing differences in physical activity, sleep duration, health-related quality of life and parental distress. J Asthma. 2014 Apr;51(3):275-81. doi: 10.3109/02770903.2013.873807. Epub 2014 Jan 10.
- Results publication: PubMed 25485038Labyak CA, Janicke DM, Lim CS, Colee J, Mathews AE. Anthropometrics to Identify Overweight Children at Most Risk for the Development of Cardiometabolic Disease. Infant Child Adolesc Nutr. 2013 Dec;5(6):341-346. doi: 10.1177/1941406413501379.
- Derived from this study: PubMed 31039250Janicke DM, Lim CS, Perri MG, Mathews AE, Bobroff LB, Gurka MJ, Parish A, Brumback BA, Dumont-Driscoll M, Silverstein JH. Featured Article: Behavior Interventions Addressing Obesity in Rural Settings: The E-FLIP for Kids Trial. J Pediatr Psychol. 2019 Sep 1;44(8):889-901. doi: 10.1093/jpepsy/jsz029.
- Derived from this study: PubMed 25317092Graef DM, Janicke DM, McCrae CS. Sleep patterns of a primarily obese sample of treatment-seeking children. J Clin Sleep Med. 2014 Oct 15;10(10):1111-7. doi: 10.5664/jcsm.4112.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
David M Janicke, Ph.D. principal investigator
University of Florida
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Behavioral Child Tx Contacts, Behavioral Parent-Tx Contacts and Dietary and Physical Activity Information in people with Obesity, run by University of Florida at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 20 Mar 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Child BMI Z score (time frame: 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01820338, which also lists 8 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Mar 2015.