NCT01282749CompletedNot Applicable
The Hospitals-Churches Partnership for Health Project: SisterTalk Hartford
UConn Health2 sites in 1 country322 target enrollmentStarted: October 1, 2002Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 322
- Locations
- 2
- Primary Endpoint
- weight loss
Study Overview
Brief Summary
The purpose of the SisterTalk Hartford study was to assess whether a theoretically- and scientifically-based, culturally acceptable weight loss program could be effectively translated into a faith-based program and subsequently delivered in the church to help African-American women lose weight.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •BMI of at least 25.0
- •self-identifies as Black or African-American
- •able to do mild physical activity such as walking or chair exercises
Exclusion Criteria
- •has insulin dependent diabetes
- •is pregnant, nursing, or had a baby in the past 4 months
- •has ever been treated for an eating disorder (e.g. anorexia nervosa, bulimia)
- •had a heart attack in the past 2 years requiring hospitalization
- •has ever had a stroke
- •has congestive heart failure
- •has uncontrolled hypertension
- •currently participating in another study
- •is on a doctor-prescribed diet that cannot be changed (e.g. very low protein diet for a person in liver failure)
Outcomes
Primary Outcomes
weight loss
Time Frame: assessed 4 times over 2 years, in roughly 6 mo intervals
Change in BMI
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (2)
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