Depressive Symptoms
Conditions
Keywords
Women with physical Disabilities, Secondary Conditions, Depression, Cognitive Behavioral Therapy, Consumer Control
Brief summary
More women with disabilities (30%) report feelings such as sadness, unhappiness, or depression that prevent them from being active compared to women without disabilities (8%). The contexts of the lives of WPD, which often include high rates of poverty, architectural and attitudinal barriers, and higher vulnerability to violence and abuse, contribute to this mental health disparity. To help address this disparity, the overall goals of this pilot study are to: 1)1. Develop a cognitive behavioral group therapy intervention to address the specific needs of WPD who experience depressive symptoms; and 2. Pilot-test the intervention to preliminarily evaluate its efficacy using a mixed-methods approach. The proposed and revised study outcomes were derived from our previous work with WPD as well as from feedback obtained from community meetings conducted since our last submission of this proposal. A pilot of the modified intervention with a total of 90 participants will be conducted using a using a wait list control design. The decision to use a wait list control design was made jointly with our community partners to ensure that all WPD participating in the study have access to the intervention.
Detailed description
The project will use a longitudinal mixed method research design. Phase I will utilize focus groups conducted with WPD to support development of the group therapy program. Phase II will evaluate the efficacy of the intervention using a randomized design. Measures to protect human subjects include development of detailed safety and referral protocols including 24 hour access to emergency mental health assessment and intervention as needed.
Interventions
BEHAVIORALWPD and Depression Treatment Group
Intervention selected will depend on Phase I data analysis.
Sponsors
U.S. Department of Education
Oregon Health and Science University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Women with physical disabilities age 18 and older who require some form of accommodation and experience significant depressive symptoms as defined by a cut off score of 16 or greater on the CES-D.
Exclusion criteria
* Women currently receiving other psychotherapy treatment * Women who are psychotic or have significant cognitive impairment * Women who are actively suicidal with intent and plan * Women who have discontinued or initiated antidepressant medications within an 4 week time period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The following hypothesis is specific to the primary outcome: Hypotheses: 1. WPD receiving the intervention will demonstrate a greater improvement in depressive symptom scores compared to participants in the wait-list control groups. | 3 years |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Outcomes: Hypothesis 2: the intervention group will demonstrate a greater improvement in coping and problem-solving skills, health behavior, body image and sexual self-esteem and loneliness compared to wait-listed controls. | 3 years |
Countries
United States
Outcome results
None listed