Morbid ObesityNCT01105156
Outcomes of Gastric Band Fills as Found With a Patient Self-reported Questionnaire: The Vomiting, Eating, and Weight Loss (VEW) Questionnaire
An observational study of Morbid Obesity, run by North Eastern Weight Loss Surgery at 1 site in Australia.
Trial summary
1. Background / Scientific Rationale The VEW (Vomiting, Eating, and Weight Loss) Questionnaire has been developed as a method for the assessment of post bariatric surgery patients, as well as a research tool into the eating behaviour of these patients. Read more about this study
- Who is it for?
- Ages 16 to 70 years
- Conditions the study is for
- Morbid Obesity
- What is being tested?
- VEW Questionnaire
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 361 participants
- Where
- 1 siteAustralia
- Study dates
- Apr 2010to Apr 2010
- Phase
- Observational
- 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 16 to 70 years
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: All patients who have received a Swedish Adjustable Gastric band at North Eastern Weight Loss Surgery
Who may be able to join
- Patients who have received a Swedish Adjustable Gastric gastric band
Who cannot join
- Patients who haven't received a Swedish Adjustable Gastric Band
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Outcomes of Gastric Band Fills as Found With a Patient Self-reported Questionnaire. The VEW [Vomiting, Eating, and Weight Loss] Questionnaire
- Background / Scientific Rationale
The VEW (Vomiting, Eating, and Weight Loss) Questionnaire has been developed as a method for the assessment of post bariatric surgery patients, as well as a research tool into the eating behaviour of these patients.
Read more
Objective VEW Questionnaire Premise If used optimally the VEW score is a valuable tool for patients who have had Laparoscopic Gastric Band Surgery (LAGB). The VEW score will be able to assist clinicians treating patients with a LAGB, specifically the Swedish Adjustable Gastric Band (SAGB), by providing them a tool to enhance patient outcomes. By using the information gained from the VEW questionnaire we can assess many areas of the eating behavior, and adjustment outcomes in patients with Gastric Bands.
Hypotheses:
- The VEW questionnaire aids in the assessment of the need for gastric band adjustment (up or down in volume)
- Comparison of patient factors in those who have had a
- good outcome (increased weight loss)
- bad outcomes (vomiting, low weight loss, maladaption), from a gastric band fluid addition
- In patients who have had a bad outcome, which factors are more predictive?
- Fewer Complications associated with Gastric Band Adjustments
- Obstruction
- Need for urgent deflation
- Pain on eating
- Lowering incidence of inappropriate fills
- Lower incidence of maladaption
- Eating behavior can predict long term outcomes
- By comparison of factors in the different quartiles of weight loss (particularly top 25% cf. bottom 25%)
- Maintenance of weight loss after 12 months is best achieved by use of behavior modification via improved food tolerances and better eating behavior than by increasing restriction of the band by further adjustments. 12 months is chosen as an arbitrary time where the majority of expected weight loss (45% of expected 50-55% 0f EWL) has been achieved. It is also a time frame by which patients have learnt to use the band appropriately, and the gastric band has had time to be adjusted into its optimal range.
- The VEW questionnaire can help predict poor outcomes from a SAGB adjustment.
- By analyzing the factors in patients who have returned both acutely (days) or at subsequent visits (weeks) and had fluid removed from their bands. These factors would include pain, vomiting, length of meals, maladaption score, fluid added, etc.
Read the detailed description
- Background / Scientific Rationale
The VEW (Vomiting, Eating, and Weight Loss) Questionnaire has been developed as a method for the assessment of post bariatric surgery patients, as well as a research tool into the eating behaviour of these patients.
Objective VEW Questionnaire Premise If used optimally the VEW score is a valuable tool for patients who have had Laparoscopic Gastric Band Surgery (LAGB). The VEW score will be able to assist clinicians treating patients with a LAGB, specifically the Swedish Adjustable Gastric Band (SAGB), by providing them a tool to enhance patient outcomes. By using the information gained from the VEW questionnaire we can assess many areas of the eating behavior, and adjustment outcomes in patients with Gastric Bands.
Hypotheses:
- The VEW questionnaire aids in the assessment of the need for gastric band adjustment (up or down in volume)
- Comparison of patient factors in those who have had a
- good outcome (increased weight loss)
- bad outcomes (vomiting, low weight loss, maladaption), from a gastric band fluid addition o In patients who have had a bad outcome, which factors are more predictive?
- Fewer Complications associated with Gastric Band Adjustments o Obstruction o Need for urgent deflation
- Pain on eating
- Lowering incidence of inappropriate fills
- Lower incidence of maladaption
- Eating behavior can predict long term outcomes
- By comparison of factors in the different quartiles of weight loss (particularly top 25% cf. bottom 25%)
- Maintenance of weight loss after 12 months is best achieved by use of behavior modification via improved food tolerances and better eating behavior than by increasing restriction of the band by further adjustments. 12 months is chosen as an arbitrary time where the majority of expected weight loss (45% of expected 50-55% 0f EWL) has been achieved. It is also a time frame by which patients have learnt to use the band appropriately, and the gastric band has had time to be adjusted into its optimal range.
- The VEW questionnaire can help predict poor outcomes from a SAGB adjustment.
- By analyzing the factors in patients who have returned both acutely (days) or at subsequent visits (weeks) and had fluid removed from their bands. These factors would include pain, vomiting, length of meals, maladaption score, fluid added, etc.
- Study Population, including Inclusion/Exclusion There are 507 patients that are eligible for inclusion to this study. The patients that will be included are only those patients that are eligible for a LAGB adjustment (thus excluding preoperative and the first post-operative visit) and have presented for review by the treating surgeon (single surgeon) in the year 2009. All non-gastric band and non-SAGB gastric bands have been excluded. Assessments by dietitians and psychologists have also been excluded.
- Study Procedures Initial Patient consent for the VEW questionnaire is obtained in consultation with the treating surgeon and dietician where the expectation, benefits and knowledge are explained and confirmed. This occurs prior to the need for adjustments, that is, during the preoperative period. To date there have been no patients that have not participated with the questionnaire.
The VEW questionnaire is handed out to all eligible (please see description for eligibility in point three) upon arrival to the clinic. Patients are given five minutes to fill out the questionnaire which is then brought into the consultation with them.
Patient care and treatment is done with the strictest adherence to the Declaration of Helsinki and in the aim of developing new and better guidelines for Best Practice for the treatment of patients who have had a LAGB.
- Duration of Study Twelve months starting 1st January 2009-31st December 2009.
- Procedure Type
The VEW score study is limited to patients that have had LAGB specifically the Swedish Adjustable Gastric Band (SAGB):
- SAGB -VC
- SABG -QC
- SAGB - 2100 The VEW questionnaire is used following all bariatric procedures but the study would be limited to the above subset of patients.
- Primary / Secondary Safety and Efficacy Endpoints
Primary Efficacy Endpoints:
- Optimal gastric band adjustment tailored for the patient for no pain on eating, no obstructions and urgent deflation of the band
- Inappropriate adjustment of the LAGB
- Identify and Decrease the incidence of maladaptive eating behaviours
Secondary Efficacy Endpoints:
- Excess Weight loss at 3, 6, 12 months
- Eating behaviour at 3,6,12 months
- Incidence of Vomiting
- Fill frequency and outcome
- Statistical Analysis Plan
Due to the significant amount of data that is currently contained in the North Eastern Weightloss Surgery database I have decided to narrow the parameters to the following for this particular study:
- All patients will be broken into two arms, one control arm and one trial arm.
- The outcomes that will be looked for are:
- Number of adjustments per patient
- Efficacy of the adjustments
- Excess Weight Loss (EWL)
- Eating behaviour and its changes
- Food tolerances (as per the Moore-Bohn Food tolerance scale)
- Safety Considerations and Reporting There are no safety considerations relating tho the use of the VEW questionnaire
- Conditions
- Morbid Obesity
- Being tested
- VEW Questionnaire
- Keywords
- Gastric band, Questionnaire, Post operative management, Adjustment
- Medical subject headings
- Obesity, Morbid
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
VEW QuestionnaireBehavioural
Also called NEWLS Questionnaire
Patient Self reported questionnaire filled in.
| Study group | Role | What they receive |
|---|---|---|
| Gastric Band Patients | Not described Receives: Behavioral: VEW Questionnaire |
What is being measured
The primary outcome is the main question the study is designed to answer.
Weight Loss
Measured: 1 year
Secondary outcomes (3)
Vomiting Frequency
Measured: 12 months
Maladaptive eating
Evaluation of any change in dietary habits
Measured: 12 months
Gastric Band adjustments
Number of adjustments
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Apr 2010 (estimated)
- Study startApr 2010
- Primary completionApr 2010 (estimated)
- Study completionApr 2010 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Morbid ObesityStudies of the same condition, open and under way.
- 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
- Observational
- Observational model
- Case only
- Time perspective
- Retrospective
- Enrolment
- 361 participants (estimated)
Sponsor and investigators
- Lead sponsor
- North Eastern Weight Loss Surgery
- Sponsor type
- University, hospital or other
- Collaborators
- Ethicon Endo-Surgery
- Investigators
- Patrick M Moore, MBBS FRACS, Principal investigator, North Eastern Weight Loss Surgery
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01105156
- Sponsor's protocol ID
- NEWLS29401
- Status last verified
- Apr 2010
- First submitted
- 13 Apr 2010
- Last updated
- 16 Apr 2010
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Apr 2010. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Outcomes of Gastric Band Fills as Found With a Patient Self-reported Questionnaire. The VEW [Vomiting, Eating, and Weight Loss] Questionnaire
- ClinicalTrials.gov ID
- NCT01105156
- Acronym / sponsor ID
- NEWLS29401
- Conditions
- Morbid Obesity
- Keywords
- Gastric band, Questionnaire, Post operative management, Adjustment
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 361 participants (estimated)
- Lead sponsor
- North Eastern Weight Loss SurgeryUniversity, hospital or other
- Collaborators
- Ethicon Endo-Surgery
- Study start
- Apr 2010
- Primary completion
- Apr 2010 (estimated)
- Study completion
- Apr 2010 (estimated)
- First posted
- 16 Apr 2010 (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.
- Background / Scientific Rationale
The VEW (Vomiting, Eating, and Weight Loss) Questionnaire has been developed as a method for the assessment of post bariatric surgery patients, as well as a research tool into the eating behaviour of these patients.
Objective VEW Questionnaire Premise If used optimally the VEW score is a valuable tool for patients who have had Laparoscopic Gastric Band Surgery (LAGB). The VEW score will be able to assist clinicians treating patients with a LAGB, specifically the Swedish Adjustable Gastric Band (SAGB), by providing them a tool to enhance patient outcomes. By using the information gained from the VEW questionnaire we can assess many areas of the eating behavior, and adjustment outcomes in patients with Gastric Bands.
Hypotheses:
- The VEW questionnaire aids in the assessment of the need for gastric band adjustment (up or down in volume)
- Comparison of patient factors in those who have had a
- good outcome (increased weight loss)
- bad outcomes (vomiting, low weight loss, maladaption), from a gastric band fluid addition
- In patients who have had a bad outcome, which factors are more predictive?
- Fewer Complications associated with Gastric Band Adjustments
- Obstruction
- Need for urgent deflation
- Pain on eating
- Lowering incidence of inappropriate fills
- Lower incidence of maladaption
- Eating behavior can predict long term outcomes
- By comparison of factors in the different quartiles of weight loss (particularly top 25% cf. bottom 25%)
- Maintenance of weight loss after 12 months is best achieved by use of behavior modification via improved food tolerances and better eating behavior than by increasing restriction of the band by further adjustments. 12 months is chosen as an arbitrary time where the majority of expected weight loss (45% of expected 50-55% 0f EWL) has been achieved. It is also a time frame by which patients have learnt to use the band appropriately, and the gastric band has had time to be adjusted into its optimal range.
- The VEW questionnaire can help predict poor outcomes from a SAGB adjustment.
- By analyzing the factors in patients who have returned both acutely (days) or at subsequent visits (weeks) and had fluid removed from their bands. These factors would include pain, vomiting, length of meals, maladaption score, fluid added, etc.
Detailed description
- Background / Scientific Rationale
The VEW (Vomiting, Eating, and Weight Loss) Questionnaire has been developed as a method for the assessment of post bariatric surgery patients, as well as a research tool into the eating behaviour of these patients.
Objective VEW Questionnaire Premise If used optimally the VEW score is a valuable tool for patients who have had Laparoscopic Gastric Band Surgery (LAGB). The VEW score will be able to assist clinicians treating patients with a LAGB, specifically the Swedish Adjustable Gastric Band (SAGB), by providing them a tool to enhance patient outcomes. By using the information gained from the VEW questionnaire we can assess many areas of the eating behavior, and adjustment outcomes in patients with Gastric Bands.
Hypotheses:
- The VEW questionnaire aids in the assessment of the need for gastric band adjustment (up or down in volume)
- Comparison of patient factors in those who have had a
- good outcome (increased weight loss)
- bad outcomes (vomiting, low weight loss, maladaption), from a gastric band fluid addition o In patients who have had a bad outcome, which factors are more predictive?
- Fewer Complications associated with Gastric Band Adjustments o Obstruction o Need for urgent deflation
- Pain on eating
- Lowering incidence of inappropriate fills
- Lower incidence of maladaption
- Eating behavior can predict long term outcomes
- By comparison of factors in the different quartiles of weight loss (particularly top 25% cf. bottom 25%)
- Maintenance of weight loss after 12 months is best achieved by use of behavior modification via improved food tolerances and better eating behavior than by increasing restriction of the band by further adjustments. 12 months is chosen as an arbitrary time where the majority of expected weight loss (45% of expected 50-55% 0f EWL) has been achieved. It is also a time frame by which patients have learnt to use the band appropriately, and the gastric band has had time to be adjusted into its optimal range.
- The VEW questionnaire can help predict poor outcomes from a SAGB adjustment.
- By analyzing the factors in patients who have returned both acutely (days) or at subsequent visits (weeks) and had fluid removed from their bands. These factors would include pain, vomiting, length of meals, maladaption score, fluid added, etc.
- Study Population, including Inclusion/Exclusion There are 507 patients that are eligible for inclusion to this study. The patients that will be included are only those patients that are eligible for a LAGB adjustment (thus excluding preoperative and the first post-operative visit) and have presented for review by the treating surgeon (single surgeon) in the year 2009. All non-gastric band and non-SAGB gastric bands have been excluded. Assessments by dietitians and psychologists have also been excluded.
- Study Procedures Initial Patient consent for the VEW questionnaire is obtained in consultation with the treating surgeon and dietician where the expectation, benefits and knowledge are explained and confirmed. This occurs prior to the need for adjustments, that is, during the preoperative period. To date there have been no patients that have not participated with the questionnaire.
The VEW questionnaire is handed out to all eligible (please see description for eligibility in point three) upon arrival to the clinic. Patients are given five minutes to fill out the questionnaire which is then brought into the consultation with them.
Patient care and treatment is done with the strictest adherence to the Declaration of Helsinki and in the aim of developing new and better guidelines for Best Practice for the treatment of patients who have had a LAGB.
- Duration of Study Twelve months starting 1st January 2009-31st December 2009.
- Procedure Type
The VEW score study is limited to patients that have had LAGB specifically the Swedish Adjustable Gastric Band (SAGB):
- SAGB -VC
- SABG -QC
- SAGB - 2100 The VEW questionnaire is used following all bariatric procedures but the study would be limited to the above subset of patients.
- Primary / Secondary Safety and Efficacy Endpoints
Primary Efficacy Endpoints:
- Optimal gastric band adjustment tailored for the patient for no pain on eating, no obstructions and urgent deflation of the band
- Inappropriate adjustment of the LAGB
- Identify and Decrease the incidence of maladaptive eating behaviours
Secondary Efficacy Endpoints:
- Excess Weight loss at 3, 6, 12 months
- Eating behaviour at 3,6,12 months
- Incidence of Vomiting
- Fill frequency and outcome
- Statistical Analysis Plan
Due to the significant amount of data that is currently contained in the North Eastern Weightloss Surgery database I have decided to narrow the parameters to the following for this particular study:
- All patients will be broken into two arms, one control arm and one trial arm.
- The outcomes that will be looked for are:
- Number of adjustments per patient
- Efficacy of the adjustments
- Excess Weight Loss (EWL)
- Eating behaviour and its changes
- Food tolerances (as per the Moore-Bohn Food tolerance scale)
- Safety Considerations and Reporting There are no safety considerations relating tho the use of the VEW questionnaire
Study design
- Observational model
- Case only
- Time perspective
- Retrospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Gastric Band Patients | – | Behavioral: VEW Questionnaire |
Who may qualify
- Ages
- 16 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- All patients who have received a Swedish Adjustable Gastric band at North Eastern Weight Loss Surgery
Key inclusion criteria (1 listed)
- Patients who have received a Swedish Adjustable Gastric gastric band
Key exclusion criteria (1 listed)
- Patients who haven't received a Swedish Adjustable Gastric Band
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 |
|---|---|---|
| VEW QuestionnaireAlso: NEWLS QuestionnairePatient Self reported questionnaire filled in. | Behavioural | Gastric Band Patients |
Primary outcome
Weight Loss
Time frame: 1 year
3 secondary outcomes
Vomiting Frequency
Time frame: 12 months
Maladaptive eating
Time frame: 12 months
Gastric Band adjustments
Time frame: 12 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Apr 2010.
Related trials for Morbid Obesity
Not yet recruitingObservational study
Pilot Study on the Effectiveness and Safety of OPTILENE® SILVER MESH ELASTIC in Prevention of Surgical Site Infection (SSI) and Incisional Hernia (IH)
Abdominal Aortic Aneurysm, Morbid Obesity
Not yet recruitingObservational study
Evaluating Metabolic Health in Individuals With Extreme Obesity
BMI>40
Enrolling by invitationObservational study
Bariatric Surgery Registry
Obesity, Morbid
Not yet recruitingObservational study
Serum Estradiol and Endometrial Thickness After Bariatric Surgery in Postmenopausal Women With Obesity
Obesity, Morbid, Postmenopause
Active, not recruiting
Mindfulness Based Eating Awareness Training for Bariatric Surgery Patients
Obesity, Morbid, Eating Disorder Symptom
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.
Patrick M Moore, MBBS FRACS principal investigator
North Eastern Weight Loss Surgery
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Morbid Obesity, run by North Eastern Weight Loss Surgery at 1 site in Australia.
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 1 inclusion and 1 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: status not confirmed, as of the sponsor's last update on 16 Apr 2010. 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 Australia. 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?
Results are not available in the source record.
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?
Weight Loss (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 16 Apr 2010.