Inpatient Obesity Intervention With Phone Follow-up
Not Applicable
Completed
- Conditions
- Obesity
- Interventions
- Behavioral: Inpatient weight loss counselingBehavioral: Motivational interviewing and troubleshooting via phone
- Registration Number
- NCT01920620
- Lead Sponsor
- Northwestern University
- Brief Summary
In this study we sought to determine whether inpatient weight loss counseling with post discharge phone follow-up would result in weight loss at six months. Secondary endpoints included weight change from baseline, changes in waist-to-hip ratios, assessment of weight perceptions and changes in patient reported health outcome measures. To our knowledge, this is the first randomized trial designed to evaluate the effects of an obesity intervention with post-discharge follow-up in an inpatient general medicine population.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 176
Inclusion Criteria
- Adults ages 18-65 years old
- Body mass index between 30-50 kg/m2
- Admitted to an internal medicine service
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Exclusion Criteria
- acute medical conditions known to affect weight (heart failure, cirrhosis, end-stage renal disease on dialysis, nephrotic syndrome, or pregnancy)
- Charlson comorbidity index >3
- moderate to severe major depression
- prolonged steroid use (>2 weeks)
- initiation of medications known to affect weight
- non-English speaking
- precontemplation stage of change
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention Arm Motivational interviewing and troubleshooting via phone Inpatient weight loss counseling Motivational interviewing and troubleshooting via phone Intervention Arm Inpatient weight loss counseling Inpatient weight loss counseling Motivational interviewing and troubleshooting via phone
- Primary Outcome Measures
Name Time Method Weight loss between groups 6 months
- Secondary Outcome Measures
Name Time Method Weight loss from baseline 6 months Change in waist-to-hip ratios 6 months Change in Patient Reported Outcomes Measurement Information System (PROMIS) scores 6 months
Trial Locations
- Locations (1)
Northwestern University
🇺🇸Chicago, Illinois, United States