Increasing Uptake of Behavioral Weight Loss Programs Among Primary Care Patients

Not Applicable

Completed

• Conditions: Obesity
• Interventions: Other: Comparator Intervention; Behavioral: Motivational Intervention

• Registration Number: NCT02708121
• Lead Sponsor: University of Florida

Brief Summary

This pilot trial will test feasibility and acceptability of a primary care-based intervention that aims to increase the portion of patients who enter evidence-based behavioral weight loss treatment.

Detailed Description

This trial is a pilot, pragmatic cluster randomized trial conducted in primary care clinics to determine intervention acceptability and the feasibility of proposed study protocol.

Study Timeline

• Study First Submitted: 2016-03-10
• Study First Submitted QC: 2016-03-10
• Study First Posted: 2016-03-15
• Study Start: 2017-03-03
• Primary Completion: 2018-02-23
• Study Completion: 2018-02-23
• Results First Submitted: 2019-01-02
• Results First Submitted QC: 2019-01-23
• Results First Posted: 2019-02-15
• Status Verified: 2019-06
• Last Update Submitted: 2019-06-21
• Last Update Posted: 2019-06-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Comparator Arm	Comparator Intervention	Participant receives access to weight loss treatment alone.
Intervention arm	Motivational Intervention	Participant receives intervention to motivate weight loss treatment initiation and access to weight loss treatment.

Primary Outcome Measures

Name	Time	Method
Number of Participants Attending 6 Month Follow-up Appointment	6 months	Count of enrolled participants who attend 6 month follow-up appointment

Secondary Outcome Measures

Name	Time	Method
Intervention Acceptability (Acceptability Outcome)	1 month	Ratings on series of items developed by study team to assess patient perception of acceptability of the intervention. Items were created by study team. Possible range of 1 (strongly disagree) to 5 (strongly agree). Higher score reflects greater acceptability except for item 11.

Trial Locations

Locations (1)

Duke University Medical Center; 🇺🇸 Durham, North Carolina, United States