NCT00056485

Brief Summary

This study will implement a treatment for depression in a nursing home setting.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25

participants targeted

Target at below P25 for not_applicable depression

Timeline
Completed

Started Apr 2002

Longer than P75 for not_applicable depression

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2002

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

March 14, 2003

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 17, 2003

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2006

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2006

Completed
Last Updated

April 13, 2017

Status Verified

April 1, 2017

Enrollment Period

4.3 years

First QC Date

March 14, 2003

Last Update Submit

April 11, 2017

Conditions

Depression

Keywords

Nursing homesAging

Interventions

Pleasant Events-Based Behavioral InterventionBEHAVIORAL

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Nursing home residents
  • DSM-IV criteria for major depressive disorder or dysthymia or Research Diagnostic Criteria for minor depressive disorder with current Geriatric Depression Scale scores \> 11 and Mini Mental State scores \>= 14

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Louisville

Louisville, Kentucky, 40292, United States

Location

MeSH Terms

Conditions

Depression

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Study Officials

  • Suzanne Meeks, PhD

    University of Louisville

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: This was a pilot feasibility study; the first part was a single group; the second part was a two-group randomized design.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

March 14, 2003

First Posted

March 17, 2003

Study Start

April 1, 2002

Primary Completion

August 1, 2006

Study Completion

August 1, 2006

Last Updated

April 13, 2017

Record last verified: 2017-04

Data Sharing

IPD Sharing
Will not share

Locations

US(1)