Weight Management and Health Behavior Intervention in Lowering Cancer Risk for BRCA Positive and Lynch Syndrome Families
NCT ID: NCT04125914
Last Updated: 2025-11-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
384 participants
INTERVENTIONAL
2017-01-26
2026-04-30
Brief Summary
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Detailed Description
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I. Identify the most effective intervention components for weight loss (primary outcome) and percent energy from fat, vegetable and fruit consumption, physical activity, and theory based behavioral determinants (secondary outcomes), with the goal of developing an optimized weight management intervention for hereditary breast and ovarian cancer (HBOC) and Lynch syndrome (LS) mutation carriers and their family members.
II. Identify the most effective intervention combination that could be delivered for a cost of $364 or less, which is the reimbursement level provided by Medicare for 6 months of intensive behavioral weight loss counseling.
III. Explore the effects of each component on weight loss, vegetable and fruit consumption, percent energy from fat, and physical activity 4 months after the end of the intervention.
IV. Evaluate whether the effects of the intervention components differ by mutation status, previous cancer diagnosis in the index participant, HBOC versus (vs) LS, family environment, and gender of index participant.
V. Pilot test the intervention in MD Anderson's Cancer Prevention Center, to determine the feasibility of providing the intervention components in a clinical setting.
OUTLINE:
Participants are randomized to 1 of 24 conditions, each comprising weight management and health behavior intervention with different combinations of 4 components for 16 weeks. The 4 components are: telephone coaching vs email coaching vs no coaching, text messages vs no text messages, self-monitoring 4-7 days a week vs 1 day per week, and a family team intervention vs none.
TELEPHONE COACHING: Participants receive 1 phone call each week from a coach over 30-45 minutes to discuss diet, physical activity and goal setting.
EMAIL COACHING: Participants receive 1 phone call to discuss the process over 10-15 minutes and then receive 1 email each week for 16 weeks.
NO COACHING: Participants receive 1 phone call the first week over 10-15 minutes to discuss the process.
TEXT MESSAGING: Participants receive 7-12 text messages comprising information about diet and physical activity each week for 16 weeks.
SELF-MONITORING: Participants record their food intake and weight directly into the Fitbit website or application 4-7 days each week or 1 day each week for 16 weeks.
FAMILY TEAM INTERVENTION: Participants (patients and their family members) receive 2 group phone calls and join a Facebook group that is monitored by research staff where they can interact with each other and coaches. The Facebook group includes weekly updates on team progress, weekly family challenges and live online chats with a dietitian and exercise expert.
After completion of study, patients are followed up at 4 and 8 months.
Conditions
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Study Design
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RANDOMIZED
FACTORIAL
PREVENTION
NONE
Study Groups
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Prevention (weight management, health behavior intervention)
Participants undergo weight management and health behavior intervention with a combination of 4 components for 16 weeks. TELEPHONE COACHING: Participants receive 1 phone call each week from a coach over 30-45 minutes to discuss diet, physical activity and goal setting. EMAIL COACHING: Participants receive 1 phone call to discuss the process over 10-15 minutes and then receive 1 email each week for 16 weeks. NO COACHING: Participants receive 1 phone call the first week over 10-15 minutes to discuss the process. TEXT MESSAGING: Participants receive 7-12 text messages comprising information about diet and physical activity each week for 16 weeks. SELF-MONITORING: Participants record their food intake and weight directly into the Fitbit website or application 4-7 days each week or 1 day each week for 16 weeks. FAMILY TEAM INTERVENTION: Participants receive 2 group phone calls and join a Facebook group that is monitored by research staff where they can interact with each other and coaches.
Behavioral Dietary Intervention
Record food intake
Receive e-mails
Exercise Intervention
Undergo exercise
Health Promotion and Education
Receive text messages
Internet-Based Intervention
Join Facebook page
Questionnaire Administration
Ancillary studies
Telephone-Based Intervention
Receive telephone coaching
Interventions
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Behavioral Dietary Intervention
Record food intake
Receive e-mails
Exercise Intervention
Undergo exercise
Health Promotion and Education
Receive text messages
Internet-Based Intervention
Join Facebook page
Questionnaire Administration
Ancillary studies
Telephone-Based Intervention
Receive telephone coaching
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* HEALTH4Families only: Index participant ONLY: Must have at least one family member who is eligible and consents to participation.
* Have at least one of the following risk factors:
* Body mass index (BMI) of 25 or higher
* \< 5 servings of vegetables and fruits per day
* \< 150 minutes per week of moderate intensity activity
* 75 minutes per week of vigorous intensity activity
* Able to read and write English.
* Have a cellular telephone and are able and willing to send and receive text messages.
* Access to internet via desktop or mobile device.
* Capable of participating in moderate-vigorous unsupervised exercise.
* HEALTH4CPC only: Patient in MD Anderson's Cancer Prevention Center coming in to the clinic for one of the following appointment types: consult and new patient screening appointments
* HEALTH4CPC only: Female.
* HEALTH4CPC only: Lives in the Houston area or surrounding counties (within 150 miles of MD Anderson's main campus).
* HEALTH4CPC only: Has a smartphone.
Exclusion Criteria
* Women who are pregnant or nursing (by self-report).
* Currently receiving radiation therapy or cytotoxic chemotherapy.
* Within 3 months of major surgery.
* Does not live in the United States.
* HEALTH4CPC only: Persons diagnosed with any invasive cancer excluding non-melanoma skin cancer.
* HEALTH4CPC only: Patient at high risk for cancer.
* HEALTH4CPC only: Participated in the HEALTH 4 MD Anderson pilot study (protocol 2014-0230).
18 Years
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Karen M Basen-Engquist
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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M D Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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MD Anderson Cancer Center Website
Other Identifiers
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NCI-2019-02453
Identifier Type: REGISTRY
Identifier Source: secondary_id
2016-0775
Identifier Type: OTHER
Identifier Source: secondary_id
2016-0775
Identifier Type: -
Identifier Source: org_study_id
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