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Inpatient Obesity Intervention With Phone Follow-up

Not Applicable
Completed
Conditions
Obesity
Interventions
Behavioral: Inpatient weight loss counseling
Behavioral: 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
GroupInterventionDescription
Intervention ArmMotivational interviewing and troubleshooting via phoneInpatient weight loss counseling Motivational interviewing and troubleshooting via phone
Intervention ArmInpatient weight loss counselingInpatient weight loss counseling Motivational interviewing and troubleshooting via phone
Primary Outcome Measures
NameTimeMethod
Weight loss between groups6 months
Secondary Outcome Measures
NameTimeMethod
Weight loss from baseline6 months
Change in waist-to-hip ratios6 months
Change in Patient Reported Outcomes Measurement Information System (PROMIS) scores6 months

Trial Locations

Locations (1)

Northwestern University

🇺🇸

Chicago, Illinois, United States

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