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NCT00056316 · ClinicalTrials.gov registry record · Phase 1
Reducing Depression in Dementia Caregivers
A Phase 1 study of Depression, sponsored by University of Missouri, St. Louis.
- Completed
- Registry status
- Phase 1
- Development phase
- 74
- Enrollment target
- 1
- Study location
NCT00056316: Completed Phase 1 study of Depression, sponsored by University of Missouri, St. Louis.
NCT00056316 is a Phase 1 study of Depression that has completed, run by University of Missouri, St. Louis. The registered enrollment target is 74 participants, below the 786-participant average among 679 other Depression trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00056316, a Phase 1 study of Depression, has completed, sponsored by University of Missouri, St. Louis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 74 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study was to develop and examine the initial impact of a distance-based intervention for female family dementia caregivers. As stated in the original proposal, the primary hypothesis of the study was that family caregivers who participated in the Video Intervention would show greater reduction in psychological distress (i.e., on measures of depression and emotional distress following problematic patient behaviors) compared to those in the Basic Education condition, and that this effect would be maintained over time (3 and 6 months post-tx).
Conditions Studied
Interventions
- BEHAVIORAL Basic Education
- BEHAVIORAL Behavioral Skills Training: Experimental
Study Locations (1)
Missouri
- University of Missouri-St. Louis - St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2002-01 |
| Est. Completion | 2004-08 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00056316
The ClinicalTrials.gov registry entry for NCT00056316 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 74 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 786-participant average among 679 other Depression trials with a reported enrollment target (91% lower). The listed sponsor is University of Missouri, St. Louis, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Depression appearing as the primary indexed condition, and to 2 interventions - of which Basic Education is the first listed.
NCT00056316 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.
Frequently Asked Questions
What is clinical trial NCT00056316 about?
NCT00056316 is a clinical study titled "Reducing Depression in Dementia Caregivers". The purpose of this study was to develop and examine the initial impact of a distance-based intervention for female family dementia caregivers. As stated in the original proposal, the primary hypothesis of the study was that family caregivers who participated in the Video Intervention would show gre...
What is the current status of trial NCT00056316?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 74 participants. The study started on 2002-01. Estimated completion is 2004-08.
What conditions does trial NCT00056316 study?
This clinical trial studies the following conditions: Depression.
What interventions are being tested in trial NCT00056316?
The interventions under investigation include: Basic Education (BEHAVIORAL), Behavioral Skills Training: Experimental (BEHAVIORAL).
Who is sponsoring clinical trial NCT00056316?
This trial is sponsored by University of Missouri, St. Louis, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00056316 being conducted?
This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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