The Weight-Wise Weight Loss Translation Study

NCT01141348 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 189

Last updated 2010-06-10

No results posted yet for this study

Summary

The overall goal of the translational research is to evaluate the processes and outcomes of implementing, in a range of public health agencies, an intense, evidence-based behavioral weight loss intervention with demonstrated effectiveness among midlife low-income women. The intervention was originally studied in a single coordinated community health care center/church setting and delivered by research staff. The investigators will evaluate the intervention's translation and test its effectiveness as implemented by existing staff in six public health agencies supported by local community resources.

Conditions

Interventions

BEHAVIORAL

Special Intervention

16 week behavioral weight loss intervention included 2 hour weekly group sessions

BEHAVIORAL

Delayed Intervention

During the randomized controlled trial, the Delayed Intervention (DI) group received two newsletters with study updates and general health information. Following the trial, the DI group received a 10-week weight loss program.

Sponsors & Collaborators

  • Centers for Disease Control and Prevention

    collaborator FED
  • Davidson County Health Department

    collaborator UNKNOWN
  • Forsyth County Health Department

    collaborator UNKNOWN
  • Lincoln County Health Department

    collaborator UNKNOWN
  • Nash County Health Department

    collaborator UNKNOWN
  • Albemarle Regional Health Services

    collaborator UNKNOWN
  • Warren County Health Department

    collaborator UNKNOWN
  • University of North Carolina, Chapel Hill

    lead OTHER

Principal Investigators

  • Carmen Samuel-Hodge, PhD, MS, RD · University of North Carolina, Chapel Hill

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
64 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2010-01-31
Completion
2010-01-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01141348 on ClinicalTrials.gov