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Reducing Obesity Using Social Ties Program

Reducing Obesity Using Social Ties (ROBUST): Randomized Control Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06335810
Acronym
ROBUST
Enrollment
264
Registered
2024-03-28
Start date
2024-04-05
Completion date
2026-12-31
Last updated
2026-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Weight Loss, Undermining, Communication

Brief summary

This trial aims to test the feasibility and acceptability of addressing interpersonal barriers to weight-related behavior change. Specifically, the study will test if, by including up to two friends, family members, or co-workers in a lifestyle intervention for weight loss, the person enrolled in the study loses more weight than someone whose friends, family members, or co-workers were not invited to participate.

Detailed description

The investigators will evaluate whether the ROBUST intervention not only addresses individual-level behaviors (i.e., healthy eating, increased physical activity) but also: 1. reduces social undermining as well as changes perceived health norms by activating communal coping - a behavioral process that involves thinking, communicating, and acting as if a health risk (i.e., Type 2 diabetes) is shared; and 2. dampens the harmful effects of increased interpersonal conflict on weight by teaching participants how to induce a positive affect and self-affirming mindset Participants in the control arm will receive the same number of lifestyle sessions as those randomized to the social network intervention. Participants will: 1. Be randomly assigned to either the study group, which is asked to invite up to two friends or family members to join them at three coaching sessions, or the group that does not invite anyone. 2. Receive 15 coaching sessions over 24 weeks. 3. Complete an online questionnaire about eating and physical activity habits, confidence in developing healthier habits, mood, and health habits of twelve of their closest friends and family members. 4. Complete a 3-day weekly food log and wear a provided Fitbit for at least 9 hours daily. 5. The invited friends and family members will also be asked to complete a brief questionnaire about their eating and physical activity habits when they start and end the study.

Interventions

Social Network interventions are an intentional effort to modify or use the characteristics of social networks to improve, generate, and maintain healthy behaviors among individuals and populations. This study will focus on implementing a behavioral social-network intervention to promote changes in weight loss behaviors.

The individual lifestyle intervention will serve as the control group and will implement the use of DPP based health coaching sessions to promote individual level changes in weight loss behaviors.

OTHERSocial Network Member

The social network member will serve as the friend, family member, or co-worker nominated to participate in the social network intervention by the social network intervention participant.

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Index Participant: 1. Black race or Hispanic ethnicity 2. Male or Female 18 years of age or older 3. Calculated BMI \> 30kg/m2 from objectively measured height and weight by study staff 4. Access \& willingness to use program food intake app via home computer or a smartphone 5. Ability to identify at least one adult social network member who will participate in the study * Social Network Member: 1. Male or Female 18 years of age or older 2. Access to the internet or a smartphone

Exclusion criteria

* Index Participant: 1. Active enrollment in a weight-loss program, use of weight-loss medications, or planning weight-loss surgery 2. Advanced medical illness, dementia, hospitalization, injury, or pregnancy that inhibits regular physical activity 3. Contraindications to exercise based on the Physical Activity Readiness Questionnaire or lack of clearance from a health care provider 4. Unresolved Food insecurity 5. Speaks a language other than English or Spanish * Social Network Member: 1. Speaks a language other than English or Spanish

Design outcomes

Primary

MeasureTime frame
Number of participants who have attended at least 75 percent of the behavioral coaching sessionsEnd of study (24 weeks)
Number of intervention participants who have at least one social network member engage in the studyEnd of Study (24 weeks)
Number of participants and social network members combined who complete the final study assessmentEnd of Study (24 Weeks)

Secondary

MeasureTime frameDescription
Change in positive communication and problem solving as measured by the McMaster Family Assessment Device (FAD) QuestionnaireBaseline, End of Study (24 weeks)The lowest score on the McMaster Family Assessment Device (FAD) Questionnaire a participant can receive is 60 and the highest score on the McMaster Family Assessment Device (FAD) Questionnaire a participant can receive is 240. Higher scores mean positive family communication and problem solving.
Change in weight related social normsBaseline, End of Study (24 weeks)A 5 point Likert scale that measures unhealthy weight norms. The lowest score is 7 and the highest score is 35. Higher scores mean healthy eating and physical activity weight norms.
Change in median Fitbit wear time in minutesWeekly up to 24 weeksTotal minutes spent in very active intensity during activity
Change in total caloric amounts on three-day food recordWeekly up to 24 weeksParticipants complete food records at minimum 3 days a week
Change in median number of days that the Fitbit is wornWeekly up to 24 weeks

Countries

United States

Contacts

CONTACTRosio Ramos, BS
ror2023@med.cornell.edu646-962-5037
CONTACTAnika Lewis, MS
ale4008@med.cornell.edu
PRINCIPAL_INVESTIGATORErica G Phillips, MD, MS

Weill Medical College of Cornell University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026