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Clinical Trials/NCT00788814
NCT00788814CompletedNot Applicable

Women Physical Disability and Depression: Communities Responding Now!

Oregon Health and Science University1 site in 1 country80 target enrollmentStarted: June 1, 2008Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
80
Locations
1
Primary Endpoint
Center for Epidemiologic Studies Depression Scale (CES-D)
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
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 -

Arms & Interventions

Control

Other

Control group

Intervention: Pathways (Behavioral)

Outcomes

Primary Outcomes

Center for Epidemiologic Studies Depression Scale (CES-D)

Time Frame: pre-test, post-test weeks, 12, 18, 24

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dena Hassouneh

Associate Professor

Oregon Health and Science University

Study Sites (1)

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