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Psychosocial ProblemNCT01504919

Reducing Cancer Disparities Among Latinos in Texas

A study testing Health Education, Questionnaires and Telephone Counseling Sessions in people with Psychosocial Problem, run by M.D. Anderson Cancer Center at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this research study is to learn if a wellness program can help improve diet and physical activity levels and encourage smoking cessation in Latino individuals who are overweight. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Psychosocial Problem
What is being tested?
Health Education, Questionnaires and Telephone Counseling Sessions
Could I receive a placebo?
No, everyone receives an active treatment
How many people
301 participants
Where
2 sitesUnited States
Study dates
Jan 2012to 18 Jan 2022
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 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Latino adults
  • 18 years of age or older
  • Current smoker with a history of smoking an average of at least 1 cigarette per day during the last year
  • Overweight/obese (BMI greater than or equal to 25)
  • Functioning telephone number
  • Valid home address
Show all 9Show fewer
  • Ability to engage in low to moderate physical activity as determined by the Physical Activity Readiness Questionnaire (PAR-Q)
  • Blood Pressure readings <140/90 mm Hg as defined by the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure; Pressure readings >/=140/90 mm Hg will be deemed ineligible to participate and excluded from the study. They will be referred to their family physician or community services. Those ineligible based on their initial blood pressure reading are allowed to participate if they provide a letter from a physician who will continue to monitor the participant during the research study.
  • Can speak, read, and understand Spanish and/or English

Who cannot join

  • Pregnancy or lactation
  • Participants who were recruited for the pilot and focus groups are not eligible for the randomized trial.
  • Contraindication for nicotine patch use
  • Regular use of tobacco products
  • Current use of tobacco cessation medications
  • Currently enrolled in another smoking cessation study
Show all 10Show fewer
  • Another household member enrolled in the study
  • Scores below 38 on the Short Assessment of Health Literacy for Spanish Adults (SAHLSA)
  • Active substance abuse or dependence
  • Scores below the 6th grade literacy level on the Rapid Estimate of Adult Literacy in Medicine (REALM)

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • William Marsh Rice University

    Houston, Texas, 77005

  • University of Texas MD Anderson Cancer Center

    Houston, Texas, 77030

Other trials in United States

About this study

The goal of this research study is to learn if a wellness program can help improve diet and physical activity levels and encourage smoking cessation in Latino individuals who are overweight.

Read the detailed description

Day 1 Study Visit:

If you are found eligible to take part in this study, the following tests and procedures will be performed on Day 1 (the same day you complete the screening tests and sign this consent form):

  • You will be asked to complete some computer-based questionnaires or paper/pencil questionnaires that will include questions about your feelings, moods, and smoking status. These will take 60-90 minutes to complete.
  • You will have your height, weight, and waistline measured.
  • Your blood pressure will be measured by a trained research staff member
  • You will complete a breath test to help researchers estimate (guess) the amount of cigarette smoke you inhale. The breath test uses a disposable cardboard tube that is attached to a machine, and you will be asked to blow a long, slow, steady breath into it.
  • You will be given an accelerometer to wear for 7 days. An accelerometer is a small device that is worn on the waistline of your pants that measures your level of physical activity. After 7 days, you will be asked to "turn off" and mail back the accelerometer using a prepaid envelope provided by the study staff.
  • You will give a saliva sample at this visit. To collect the saliva sample, you will place a piece of cotton in your mouth for 3 minutes. The saliva sample is used to check the amount of cotinine in the body. Cotinine is a chemical that is produced in your saliva when your body breaks down nicotine.

Study Groups and Study Procedures:

At the Day 1 study visit, you will be randomly assigned (as in the flip of a coin) into 1 of 2 study groups. There is an equal chance of being assigned to either group.

Participants in both groups will receive health education on Day 1, and again 6 and 12 months later. You can also ask to receive a 6-week supply of nicotine patches, whenever you are ready to try to quit smoking and a home-based exercise kit when you are ready to begin an exercise program.

At the Day 1 health education session, the following will take place:

  • You will have a brief counseling session with a study staff member to talk about smoking, diet, and your physical activity level.
  • You will be offered referrals to available resources for help with your smoking cessation, diet, and physical activity.
  • You will be given a home-based exercise kit, along with self-help materials that are designed to help you learn how to quit smoking and how to improve your diet and physical activity.

At the Months 6 and 12 health education sessions, the Day 1 activities will be repeated, and the following procedures will also take place:

  • You will complete a computer-based or paper/pencil questionnaire about your mood, diet, and physical activity. This will take 60-90 minutes to complete.
  • Your weight and waistline will be measured.
  • You will complete a breath test. The breath test uses a disposable cardboard tube that is attached to a machine, and you will be asked to blow a long, slow, steady breath into it.
  • You will give a saliva sample. To collect the saliva sample, you will place a piece of cotton in your mouth for 3 minutes. The saliva sample is used to check the amount of cotinine in the body. Cotinine is a chemical that is produced in your saliva when your body breaks down nicotine.
  • You will be given an accelerometer to wear for 7 days. After 7 days, you will mail back the accelerometer using a prepaid envelope provided by the study staff.

You will also have a follow-up study visit at Month 18. During this visit, the same procedures from the Month 12 visit will be performed. However, you will not have a health education session at Month 18.

Wellness Program:

In addition to the health education visits and materials, participants in Group 2 will also take part in the wellness program. For the wellness program, you will receive 18 counseling phone calls over the 18 months you are on study. Each of these phone calls should last about 20-30 minutes.

The telephone counseling sessions will be digitally recorded. Audio recordings will be erased once the data have been published. The recordings will be used to help the researchers make sure that the counselors are following the correct procedures and may be used in the future to help the researchers better understand or improve the counseling treatment. No one but the researchers and their staff will be allowed to view or listen to the recordings, and the identity of the participants will be kept strictly confidential. Your study identification number will be stated by the counselor at the beginning of the taped session. The recordings are stored digitally, encrypted, and password protected.

Questionnaire Data:

Your questionnaire data will be used for research purposes only. Your responses will not be shared with your doctor. If you feel you need a doctor's opinion about anything that is asked about in the questionnaires (such as mental or emotional difficulties or symptoms), please contact either your personal doctor or the study chair.

Length of Study:

You will remain on the study for up to 18 months. Your participation on this part of the study will be over once you complete the study visit at Month 18.

Other Important Information:

  • You may be contacted by phone, mail, and/or email at any time while you are taking part in this study to be reminded about the study visits. You will be asked to give the study chair the names and contact information for family members and/or friends that the study staff can contact if they cannot reach you.
  • If the accelerometer is lost or stolen, you will not be responsible for the replacement cost, but you should tell the study chair right away.

This is an investigational study. The nicotine patch is FDA approved and commercially available. Up to 500 participants overall will take part in this research study. Up to 400 participants will take part in this portion of the study. All will be enrolled at MD Anderson.

Being tested
Health Education, Questionnaires, Telephone Counseling Sessions, Nicotine Patches
Keywords
Psychosocial, Behavioral intervention, Nicotine patch, Latinos, Mexican American, Motivation and Problem Solving, MAPS, Cancer risk reduction, Smoking cessation, Overweight/obese smokers, BMI greater than or equal to 25, Wellness program, Questionnaires, Surveys, Self-help materials, Pamphlets
Medical subject headings
Smoking Cessation, Overweight

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Health EducationBehavioural

    Brief counseling at baseline, at 6 months and again at 12 months, and self-help materials addressing smoking cessation, diet, physical activity, referrals to available resources, and a home-based exercise kit (e.g., pedometer, exercise ball, strength training cables).

  • QuestionnairesBehavioural

    Also called surveys

    Computer-based questionnaires completed at baseline, then every 6 months taking 60-90 minutes to complete.

  • Telephone Counseling SessionsBehavioural

    Also called Counseling

    9 proactive, telephone counseling sessions over 18 months. Each of these phone calls should last about 20-30 minutes.

  • Nicotine PatchesDrug

    6-week supply of nicotine patches given to participants ready to quit smoking.

Study groups in NCT01504919
Study groupRoleWhat they receive
Health Education (HE)ExperimentalHE of brief counseling and self-help materials addressing 3 risk behaviors, referrals to available resources, and a home-based exercise kit; 6-week supply of nicotine patches for smoking cessation if needed.
Receives: Behavioral: Health Education; Behavioral: Questionnaires; Drug: Nicotine Patches
Motivation and Problem Solving (MAPS)ExperimentalHE counseling, self-help materials, and resource referrals, and home-based exercise kit; 6-week supply of nicotine patches for smoking cessation if needed. Plus 9 proactive, telephone counseling sessions over the 18 month period.
Receives: Behavioral: Health Education; Behavioral: Questionnaires; Behavioral: Telephone Counseling Sessions; Drug: Nicotine Patches

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Efficacy of Motivation and Problem Solving (MAPS) in Cancer Risk Reduction

    Generalized linear mixed model regression (GLMM) used in analyzing the effects of motivation and problem solving (MAPS) on the primary outcomes across the 6, 12, and 18-month time points.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Jan 2012 (estimated)
  2. Study startJan 2012
  3. Primary completion18 Jan 2022
  4. Study completion18 Jan 2022

Resources

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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
301 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01504919
Sponsor's protocol ID
2010-0606
Other IDs
NCI-2012-00029, 5U54CA153505
Status last verified
May 2022
First submitted
3 Jan 2012
Last updated
31 May 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Castro Y, Basen-Engquist K, Fernandez ME, Strong LL, Eakin EG, Resnicow K, Li Y, Wetter DW. Design of a randomized controlled trial for multiple cancer risk behaviors among Spanish-speaking Mexican-origin smokers. BMC Public Health. 2013 Mar 18;13:237. doi: 10.1186/1471-2458-13-237.

    PubMed 23506397

Questions about this trial

What is this clinical trial studying?

A study testing Health Education, Questionnaires and Telephone Counseling Sessions in people with Psychosocial Problem, run by M.D. Anderson Cancer Center at 2 sites 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 9 inclusion and 10 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 31 May 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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?

Efficacy of Motivation and Problem Solving (MAPS) in Cancer Risk Reduction (time frame: 6 months). 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 NCT01504919, which also lists 1 linked publication.

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 31 May 2022.

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