Engaging Patients in Weight Loss Tools

NCT ID: NCT04121312

Last Updated: 2024-01-16

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 33 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-10-28
• Study Completion Date: 2020-07-24

Brief Summary

The overall aim of this study is to evaluate the acceptability and feasibility of a primary-care based approach to facilitating engagement in online behavior tracking and community support networks for weight loss ("facilitation condition") over 12 weeks among adults with obesity.

Conditions

Obesity

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: HEALTH_SERVICES_RESEARCH
• Blinding Strategy: NONE

Study Groups

Facilitation Intervention

A brief, web-based facilitation guide (called "Weight Loss Your Way Kickoff Materials") that encourages initial and sustained engagement in online tracking and social network tools for weight loss.The intervention also includes 8 emails sent over 12 weeks to further motivate use of the online tools and weight loss.

Group Type: EXPERIMENTAL

Facilitation Intervention

Intervention Type: BEHAVIORAL

See "arm" description

Interventions

Facilitation Intervention

See "arm" description

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• PCPs:

1. Employed as a PCP at a clinics in the UF health care system.

2. Has practiced at current clinic for ≥1 year (self-report)

3. Is employed ≥ 0.5 FTE (self-report)

4. Has a patient panel that is majority adult (self-report)

• Patients: EHR-based criteria:

1. Age 18-75

2. Last BMI in EHR ≥30 kg/m2

3. Has an appointment scheduled ("index appointment") with an enrolled primary care PCP 7-30 days after electronic data pull.

4. Is enrolled in MyChart or has an email address in the IDR system.

Self-report criteria:

5. Self-reported BMI > 29 kg/m2 (to account for under-reporting)

6. Response yes to question: "Would you be interested in learning strategies to help you lose weight?"

7. Ability to read and understand English without assistance.

8. Has either (a) a phone or tablet with a data plan OR (b) reliable access to Wi-Fi (via computer, phone or tablet) in their home.

Exclusion Criteria

• PCPs:

1. Planning to move out of the Gainesville or Jacksonville area in the next 12 months.

• Patients:

1. Currently enrolled in formal weight loss program or a research study focused on changing diet, physical activity, or weight.

2. In past month, has tracked the majority of their food intake on an app, website, or paper log an average of 3 or more days per week.

3. Self-reported to be pregnant, breastfeeding, or planning to become pregnant in next 6 months.

4. Currently undergoing radiation or chemotherapy for cancer.

5. Self-reported cardiac event in past 6 months.

6. Self-reported Heart Failure (also known as chronic heart failure or CHF).

7. Planning to move out of the Gainesville or Jacksonville area (depending on which clinic they are recruited from) in the next 6 months.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Florida

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Megan McVay, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Locations

UF Health at the University of Florida

Gainesville, Florida, United States

UF Health - Jacksonville

Jacksonville, Florida, United States

Countries

United States

Other Identifiers

OCR26064

Identifier Type: OTHER

Identifier Source: secondary_id

IRB201902013

Identifier Type: -

Identifier Source: org_study_id