Weill Cornell Medicine
New York, 10065, United States
Location status: Recruiting
Location contact
Anika Lewis, MS
CONTACT
Erica Phillips, MD, MS
CONTACT
Erica Phillips, MD, MS
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06335810
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
New York, 10065, United States
Location status: Recruiting
Anika Lewis, MS
CONTACT
Erica Phillips, MD, MS
CONTACT
Erica Phillips, MD, MS
PRINCIPAL_INVESTIGATOR
The investigators will evaluate whether the ROBUST intervention not only addresses individual-level behaviors (i.e., healthy eating, increased physical activity) but also:
Participants in the control arm will receive the same number of lifestyle sessions as those randomized to the social network intervention.
Participants will:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
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.
Time frame: End of study (24 weeks)
Time frame: End of Study (24 weeks)
Time frame: End of Study (24 Weeks)
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Weekly up to 24 weeks
Total minutes spent in very active intensity during activity
Time frame: Weekly up to 24 weeks
Participants complete food records at minimum 3 days a week
Time frame: Weekly up to 24 weeks
Contact information is provided by the study sponsor or research team.
Weill Medical College of Cornell University
Other
Reducing Obesity Using Social Ties (ROBUST): Randomized Control Trial
Acronym: ROBUST
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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