N/A
N=66
Increasing Uptake of Behavioral Weight Loss Programs Among Primary Care Patients
Obesity
Bottom Line
View on ClinicalTrials.gov: NCT02708121 ↗Enrolled (actual)
66
Serious AEs
1.7%
Results posted
Feb 2019
Primary outcome: Primary: Number of Participants Attending 6 Month Follow-up Appointment — 22; 19 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Motivational Intervention (Behavioral); Comparator Intervention (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Florida
- Primary completion
- Feb 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Attending 6 Month Follow-up Appointment |
22; 19 | — |
| SECONDARY Intervention Acceptability (Acceptability Outcome) |
4.15; 4.05; 4.25; 4.30; 4.10; 4.15 | — |
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.
Eligibility Criteria
Primary care provider Inclusion criteria:
- Employed by Duke PCRC clinic as primary care provider at least ½ FTE.
- Has a primary adult panel
- Has worked at Duke PCRC clinic for at least one year
Patient inclusion criteria
- BMI ≥ 30 kg/m2 as measured at any clinic in previous 12 months.
- English speaking
- Self-report BMI ≥ 29 kg/m2 (to allow for under-reporting)
- Regular email usage, defined as accessing email 3 or more times per week (on home or work computer or cell phone)
- Age 18-75
- Clinical appointment (well visit or chronic care visit) with enrolled Duke provider in 2-6 weeks of record review.
- At least one prior appointment with the provider they are scheduled to see at target clinical appt.
- Has a valid email address in electronic health records.
Patient exclusion criteria:
- In weight loss treatment program in past year
- Unable to read content on websites without any assistance
Data sourced from ClinicalTrials.gov (NCT02708121). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.