Study of Pathways Curriculum for Use With WPD

Sponsor
Oregon Health and Science University (Other)
Overall Status
Completed
CT.gov ID
NCT00788814
Collaborator
Portland State University (Other)
80
1
1
43
1.9

Study Details

Study Description

Brief Summary

Study to assess the efficacy of a modified Pathways curriculum in treating depressive symptoms in women with physical disabilities.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Pathways
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Women Physical Disability and Depression: Communities Responding Now!
Study Start Date :
Jun 1, 2008
Actual Primary Completion Date :
Jan 1, 2012
Actual Study Completion Date :
Jan 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Other: Control

Control group

Behavioral: Pathways
Strength-based curriculum addressing depression in women with with physical disabilities

Outcome Measures

Primary Outcome Measures

  1. Center for Epidemiologic Studies Depression Scale (CES-D) [pre-test, post-test weeks, 12, 18, 24]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Women with physical disability requiring accommodation for major mobility limitations

  • CES-D score of 16 or higher -

Exclusion Criteria:
  • Active suicidality

  • Diagnosis of Schizophrenia, Schizoaffective D/O, Psychosis NOS

  • Currently receiving other psychotherapy -

Contacts and Locations

Locations

Site City State Country Postal Code
1 Oregon Health & Science University Portland Oregon United States 97236

Sponsors and Collaborators

  • Oregon Health and Science University
  • Portland State University

Investigators

  • Principal Investigator: Dena M Hassouneh, PhD, Oregon Health and Science University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dena Hassouneh, Associate Professor, Oregon Health and Science University
ClinicalTrials.gov Identifier:
NCT00788814
Other Study ID Numbers:
  • 1R01MH079818-01A1
  • 1R01MH079818-01A1
First Posted:
Nov 11, 2008
Last Update Posted:
Oct 17, 2012
Last Verified:
Oct 1, 2012
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 17, 2012