NCT05775497

Brief Summary

Obesity disproportionately impacts sexual minority women. Behavioral weight loss programs are the gold standard treatment for mild to moderate obesity. The investigators have developed an online behavioral weight loss program that is effective, low-cost, and highly scalable. However, existing research suggests that tailoring treatment to address 3 well-established weight loss barriers in sexual minority women will be critical for maximizing the relevance and efficacy of behavioral weight loss for this group. In the Preparation Phase of this K23, the investigators developed 3 novel treatment components targeting sexual minority women's weight loss barriers (i.e., minority stress, low social support, and negative body image), the investigators piloted the program among sexual minority women of higher weight, and the investigators conducted individual qualitative interviews to elicit feedback on the intervention's acceptability, cultural relevance, usability, and feasibility, and this feedback was used to refine the program. In the Optimization Phase of this K23 (the current phase), 88 women will receive 12 weeks of Rx Weight Loss and will be randomized to receive 0-3 tailored components in a full factorial design with 23 (8) distinct combinations of components. Novel components that increase mean weight loss (by ≥2%) or the proportion of women achieving clinically meaningful weight loss (by ≥10%) at 6 months will be retained in a finalized obesity treatment package that the investigators will evaluate in a future randomized controlled trial (RCT) (Evaluation Phase). The aims of this study are to: Aim 2A (Optimization): Use a factorial experiment to determine how 3 novel components impact mean weight loss and the proportion of women achieving a 5+% weight loss at 6 months. Aim 2B (Mediation): Clarify how tailored components impact weight loss by testing hypothesized mechanisms of action (i.e., coping with stress, perceived social support, weight and shape concerns). This project will tailor and optimize an evidence-based online behavioral obesity treatment to enhance weight loss outcomes in sexual minority women.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
88

participants targeted

Target at P50-P75 for not_applicable obesity

Timeline
Completed

Started May 2024

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 28, 2023

Completed
20 days until next milestone

First Posted

Study publicly available on registry

March 20, 2023

Completed
1.1 years until next milestone

Study Start

First participant enrolled

May 1, 2024

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 29, 2025

Completed
Last Updated

December 27, 2024

Status Verified

December 1, 2024

Enrollment Period

1.3 years

First QC Date

February 28, 2023

Last Update Submit

December 23, 2024

Conditions

Keywords

Sexual minority womenLGBTQ healthWeight loss

Outcome Measures

Primary Outcomes (2)

  • Change in Weight

    Body weight will be formally assessed by an RA at baseline, 3 months, and 6 months. Mean weight loss from baseline will be calculated.

    6 months

  • Proportion of Patients Achieving a Weight Loss of 5+% of Initial Weight

    Mean weight loss at 6 months will be used to determine the proportion of participants who achieved clinically significant (5+%) weight loss.

    6 months

Secondary Outcomes (5)

  • Change in Weight

    3 months

  • Proportion of Patients Achieving a Weight Loss of 5+% of Initial Weight

    3 months

  • Change in skills for coping with stress

    3 and 6 months after baseline

  • Change in perceived social support

    3 and 6 months after baseline

  • Change in negative body image

    3 and 6 months after baseline

Other Outcomes (3)

  • Adherence to behavioral weight loss - Online metrics

    3 months after baseline

  • Adherence to behavioral weight loss - Energy intake

    3 months after baseline

  • Adherence to behavioral weight loss - Physical activity

    3 and 6 months after baseline

Study Arms (8)

Weight Loss Program Only

EXPERIMENTAL

Participants complete an online behavioral weight loss program.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)

Weight Loss Program + Coping with Stress Program

EXPERIMENTAL

Participants complete (1) an online behavioral weight loss program and (2) an adjunctive intervention that teaches strategies for coping with stress \& stigma due to weight, sexual orientation, and gender \& its impact on weight loss.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)Behavioral: Minority stress intervention

Weight Loss Program + Coping with Stress Program + Body Image Program

EXPERIMENTAL

Participants complete (1) an online behavioral weight loss program, (2) an adjunctive intervention that teaches strategies for coping with stress \& stigma due to weight, sexual orientation, and gender \& its impact on weight loss, and (3) an adjunctive intervention for improving negative body image and reducing its impact on weight loss.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)Behavioral: Minority stress interventionBehavioral: Negative body image intervention

Weight Loss Program + Coping with Stress Program + Body Image Program + Social Support Program

EXPERIMENTAL

Participants complete (1) an online behavioral weight loss program, (2) an adjunctive intervention that teaches strategies for coping with stress \& stigma due to weight, sexual orientation, and gender \& its impact on weight loss, (3) an adjunctive Social Support Intervention that provides participants with online opportunities to give and receive real-time social support for weight loss efforts, and (4) an adjunctive intervention for improving negative body image and reducing its impact on weight loss.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)Behavioral: Minority stress interventionBehavioral: Social support interventionBehavioral: Negative body image intervention

Weight Loss Program + Body Image Program + Social Support Program

EXPERIMENTAL

Participants complete (1) an online behavioral weight loss program, (2) an adjunctive Social Support Intervention that provides participants with online opportunities to give and receive real-time social support for weight loss efforts, and (3) an adjunctive intervention for improving negative body image and reducing its impact on weight loss.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)Behavioral: Social support interventionBehavioral: Negative body image intervention

Weight Loss Program + Coping with Stress Program + Social Support Program

EXPERIMENTAL

Participants complete a (1) online behavioral weight loss program, (2) an adjunctive intervention that teaches strategies for coping with stress \& stigma due to weight, sexual orientation, and gender \& its impact on weight loss, and (3) an adjunctive Social Support Intervention that provides participants with online opportunities to give and receive real-time social support for weight loss efforts.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)Behavioral: Minority stress interventionBehavioral: Social support intervention

Weight Loss Program + Body Image Program

EXPERIMENTAL

Participants complete (1) an online behavioral weight loss program and (2) an adjunctive intervention for improving negative body image and reducing its impact on weight loss.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)Behavioral: Negative body image intervention

Weight Loss Program + Social Support Program

EXPERIMENTAL

Participants complete (1) an online behavioral weight loss program and (2) an adjunctive Social Support Intervention that provides participants with online opportunities to give and receive real-time social support for weight loss efforts.

Behavioral: Behavioral weight loss intervention (Online; Rx Weight Loss)Behavioral: Social support intervention

Interventions

Rx Weight Loss is a fully automated online behavioral obesity treatment that includes 3 core components: weekly online video lessons, submission of self-monitored weight, calorie intake, and activity data, and personalized automated feedback. Participants set goals for weight loss (e.g., 10%), daily calorie intake, and activity (e.g., 200 mins/week of moderate-to-vigorous intensity physical activity). Online lessons discuss healthy eating, physical activity, and behavioral skills (e.g., stimulus control, goal-setting, problem solving). To maintain participant engagement, lessons are interactive, use audio and video, and include experiential learning opportunities. Based on their progress, participants receive automated feedback that provides encouragement, praise for meeting goals, and constructive feedback. To enhance adherence, participants who do not view the weekly lesson or enter monitoring data receive e-mail reminders to re-engage.

Weight Loss Program + Body Image ProgramWeight Loss Program + Body Image Program + Social Support ProgramWeight Loss Program + Coping with Stress ProgramWeight Loss Program + Coping with Stress Program + Body Image ProgramWeight Loss Program + Coping with Stress Program + Body Image Program + Social Support ProgramWeight Loss Program + Coping with Stress Program + Social Support ProgramWeight Loss Program + Social Support ProgramWeight Loss Program Only

The Minority Stress Intervention will teach cognitive and behavioral strategies for coping with minority stress with a focus on how minority stress impacts weight loss behaviors. The treatment will primarily address stressors due to sexuality and weight but will also cover how minority stress intersects with other facets of identity. The intervention, while innovative, is adapted from evidence-based treatments using cognitive behavioral therapy (CBT) to address minority stress.Lessons will provide psychoeducation on minority stress related to sexuality, gender, and weight, how it intersects with other aspects of identity, and how it can interfere with weight loss (e.g., unhealthy eating, avoiding exercise and healthcare, reduced motivation, disengaging from the program).The treatment will be delivered in 12 8-10-min lessons/week (a duration comparable to previous treatments) viewed directly after Rx Weight Loss lessons in Wks 1-12.

Also known as: Coping with Stress Program
Weight Loss Program + Coping with Stress ProgramWeight Loss Program + Coping with Stress Program + Body Image ProgramWeight Loss Program + Coping with Stress Program + Body Image Program + Social Support ProgramWeight Loss Program + Coping with Stress Program + Social Support Program

The Social Support Intervention will provide sexual minority women with online opportunities to give and receive real-time social support for weight loss efforts. The treatment is based on Social Learning Theory and evidence-based online social support programs used in behavioral weight loss. The intervention will include one video lesson outlining the value of social support for weight loss and well-being, strategies for eliciting support, and an orientation to using the online platform (hosted within Rx Weight Loss). The platform will feature a private forum where participants can post to provide support and discuss their weight loss goals, challenges, and successes. To foster engagement, discussion topics will be automated to post 4 times/week and those who do not participate will be reminded via e-mail to engage (1x/month).

Also known as: Social Support Program
Weight Loss Program + Body Image Program + Social Support ProgramWeight Loss Program + Coping with Stress Program + Body Image Program + Social Support ProgramWeight Loss Program + Coping with Stress Program + Social Support ProgramWeight Loss Program + Social Support Program

The Negative Body Image Intervention will teach CBT skills for improving negative body image and reducing its impact on weight loss behaviors. The treatment is derived from evidence-based CBT interventions targeting body image for women with obesity during behavioral weight loss and will be adapted to reflect the unique body image ideals and concerns of sexual minority women. Lessons will teach CBT strategies for coping with negative body image and reducing interference with weight loss efforts. The intervention will be delivered in 12 weekly 8-10-minute lessons, a treatment duration comparable to previous treatments and will be viewed immediately following Rx Weight Loss lessons during Weeks 1-12.

Also known as: Body Image Program
Weight Loss Program + Body Image ProgramWeight Loss Program + Body Image Program + Social Support ProgramWeight Loss Program + Coping with Stress Program + Body Image ProgramWeight Loss Program + Coping with Stress Program + Body Image Program + Social Support Program

Eligibility Criteria

Age18 Years - 70 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsCurrently self-identify as female
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
* Assigned female at birth and currently identify as female * Self-identify a minority sexual orientation (e.g.,lesbian, bisexual) * BMI=25-50kg/m2 * 18-70 years old * Interested in losing weight * Regular internet and e-mail access * No significant weight loss within past 6 months (\>5%) * Fluent in English * Able to participate in moderate physical activity * Not currently enrolled in a weight loss program * Not currently taking weight-loss medication * Not currently pregnant or trying to get pregnant * Participated in a previous Phase of this study * Reports a serious mental/physical health condition that would increase potential risks of treatment to the participant (e.g., active symptoms of psychosis, suicidality, mania, alcohol/substance use, or a medical condition that is serious, active, unstable, and degenerative (e.g., CHF)).

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

Study Sites (1)

Weight Control and Diabetes Research Center

Providence, Rhode Island, 02903, United States

RECRUITING

MeSH Terms

Conditions

ObesityWeight Loss

Interventions

Coping Skills

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsBody Weight Changes

Intervention Hierarchy (Ancestors)

Behavior TherapyPsychotherapyBehavioral Disciplines and Activities

Central Study Contacts

Emily Panza, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
FACTORIAL
Model Details: Participants (anticipated n=88) will receive the 12-week online weight loss treatment and will be randomized to receive 0-3 novel intervention components (targeting minority stress, negative body image, and social support). The primary outcome (weight loss) will be assessed at baseline, post-treatment (12 weeks), and follow-up (24 weeks).
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 28, 2023

First Posted

March 20, 2023

Study Start

May 1, 2024

Primary Completion

September 1, 2025

Study Completion

December 29, 2025

Last Updated

December 27, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Results will be submitted to ClinicalTrials.gov within appropriate timelines. Quantitative data will be published in peer-reviewed manuscripts that will be submitted to PubMed Central upon acceptance. Study results will be presented to the scientific community at national conferences relevant to obesity and sexual minority health. Aggregate quantitative data may be requested from other researchers 5 years after the completion of the primary endpoint by contacting Dr. Panza. If there are no restrictions imposed by institutional policies, local IRBs, or laws/regulations, the investigators will make de-identified data available to a requester within the context of a clear data-sharing agreement.

Locations