Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00788814 · ClinicalTrials.gov registry record · NA
Study of Pathways Curriculum for Use With WPD
A NA study, sponsored by Oregon Health and Science University.
- Completed
- Registry status
- NA
- Development phase
- 80
- Enrollment target
NCT00788814: Completed NA study, sponsored by Oregon Health and Science University.
NCT00788814 is a NA study that has completed, run by Oregon Health and Science University. The registered enrollment target is 80 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00788814, a NA study, has completed, sponsored by Oregon Health and Science University.
- COMPLETED
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
Study Summary
Study to assess the efficacy of a modified Pathways curriculum in treating depressive symptoms in women with physical disabilities.
Interventions
- BEHAVIORAL Pathways
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2008-06 |
| Est. Completion | 2012-01 |
| Phase | NA |
What the finished NCT00788814 record still lists
NCT00788814 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 1 intervention - of which Pathways is the first listed.
NCT00788814 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00788814 about?
NCT00788814 is a clinical study titled "Study of Pathways Curriculum for Use With WPD". Study to assess the efficacy of a modified Pathways curriculum in treating depressive symptoms in women with physical disabilities.
What is the current status of trial NCT00788814?
This trial is currently completed. It is a NA study. The enrollment target is 80 participants. The study started on 2008-06. Estimated completion is 2012-01.
What interventions are being tested in trial NCT00788814?
The interventions under investigation include: Pathways (BEHAVIORAL).
Who is sponsoring clinical trial NCT00788814?
This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00788814's enrollment target sits among peer trials
80 994th of 2000 higher than 941 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01243931 · 80 participants · NA
Optical Coherence Tomography Guided Transepithelial Phototherapeutic Keratectomy
- NCT01659203 · 80 participants · Phase 1
Proton or Photon RT for Retroperitoneal Sarcomas
- NCT01803451 · 80 participants · Early Phase 1
Glucagon-like Peptide 1, Glucose Metabolism and Gastric Bypass
- NCT01964859 · 80 participants · Phase 2
Feasibility Study for Fibroblast Autologous Skin Grafts
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia