N/A
Completed N=123
Collaborative Care for Women Veterans
Anxiety · Depression · Stress Disorders, Post Traumatic
Source: ClinicalTrials.gov NCT02950961 ↗
Enrolled (actual)
123
Serious AEs
0.0%
Results posted
Mar 2024
Primary outcomePrimary: Change in Utilization of Services (30 Days) — 53; 23; 40 Participants
Summary
Implementation of Tailored Collaborative Care for Women Veterans (CCWV) was designed to enhance primary care-mental health integration for women Veterans by tailoring services to women Veterans' and providers' needs and providing an evidence-based intervention, Coordinated Anxiety Learning and Management, to address anxiety and depression in a patient-centered approach. CCWV was implemented in two of the Women's Health Practice-Based Research Network sites, with careful attention to local tailoring and adaptation to enhance the fit of the care model in varied local contexts.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Utilization of Services (30 Days) |
53; 23; 40 | — |
| PRIMARY Change in Utilization of Services (60 Days) |
40; 14; 62 | — |
| PRIMARY Change in Utilization of Services (180 Days) |
29; 10; 77 | — |
| PRIMARY Change in Utilization of Services (365 Days) |
28; 8; 80 | — |
| PRIMARY Change in Referrals |
— | — |
| PRIMARY Patient-Reported Outcomes Measurement Information System (PROMIS) |
— | — |
| PRIMARY Overall Anxiety Severity and Impairment Scale (OASIS) |
— | — |
| PRIMARY Patient Health Questionnaire for Depression and Anxiety (PHQ-4) |
— | — |
| PRIMARY WHO Disability Assessment Schedule (WHODAS) Out Of Role Days Items |
— | — |
| PRIMARY Global Rating of Satisfaction/Quality of Care |
— | — |
| PRIMARY Altarum Consumer Engagement |
— | — |
| PRIMARY Health Literacy (Chew et al. 2004) |
— | — |
Eligibility Criteria
Inclusion Criteria
Patient Participants:
- Women VA patients with possible or confirmed anxiety and/or depression and/or PTSD
Provider Participants:
- VA staff in a primary care and/or mental health clinic
- Note: gender based inclusion criteria did not apply to provider participants
Exclusion Criteria
Patient Participants:
- Male gender
- Cognitive impairment that would preclude completion of informed consent
Provider Participants:
- None
Data sourced from ClinicalTrials.gov (NCT02950961). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.