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Engaging Patients in Weight Loss Tools

Engaging Primary Care Patients in Online Weight Management Tools: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04121312
Enrollment
33
Registered
2019-10-09
Start date
2019-10-28
Completion date
2020-07-24
Last updated
2024-01-16

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

Conditions

Obesity

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.

Interventions

BEHAVIORALFacilitation Intervention

See arm description

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Patient retention12 weeksPercent of enrolled patients completing the 12-week follow-up assessment. (NOTE: this is a feasibility pilot and is not conceptualized as having a single primary outcome)

Secondary

MeasureTime frameDescription
Percent of contacted providers who enrollNA (depends on period of recruitment, approx 1 month)Percent of PCPs offered the study who consent
Percent of patients who enrollNA (depends on period of recruitment, approx 2-4 months)Percent of patients contacted who are eligible and agree to participate.
Rate of patient recruitmentup to 16 weeksPatients recruited per month during active recruitment periods
Acceptability of intervention- providerAt end of intervention (about 4-6 months after start, depending on recruitment rate)Response to 5 study specific questions asking about alignment with priorities, fit in workflow, feasibility, perception of patient benefit, and time. Also, response to open ended question about acceptability.
Provider retention4-6 months (depends on patient recruitment rate)Percent of enrolled providers who complete telephone interview at end of study
Initial engagement in Tracking tool and social network12 weeksPortion of patients who initially engage with tracking tool (i.e., log at least one food item or physical activity) and with social network (i.e., who report reading message board or posting at least once) (tracking and social network examined separately)
Sustained engagement in Tracking tool and social network12 week assessment (queried about prior week)Portion of patients who have used the tracking tool and social network at least once in past week at 12 week assessment (tracking and social network examined separately)
Weight changebaseline to 12 weeksMean weight loss (kgs) and portion of participants achieving 3% body weight loss.
Acceptability of intervention- patient: 12 study specific questions12 weeksResponse to 12 study specific questions asking about experience with Weight Loss Your Way kickoff materials; open ended response to questions about acceptability of intervention during qualitative interviews (of portion of enrollees)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026