Reducing Depression in Dementia Caregivers

This study has been completed.

Study NCT00056316 Information provided by National Institute of Mental Health (NIMH)

First Received: March 10, 2003 Last Updated: November 17, 2008 History of Changes

Study Type:	Interventional
Study Design:	Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment
Condition:	Depression
Interventions:	Behavioral: Basic Education Behavioral: Behavioral Skills Training: Experimental

Participant Flow

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Recruitment Details

Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
Recruitment took place from 10/2001 to 3/2004. Project information was distributed to Alzheimers Association Chapters and Area Agencies on Aging (AAA's) in Midwestern USA (IO, IL,IN, KS, MI, MO, MN, NB,WI).

Pre-Assignment Details

Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
All enrolled participants who completed consent procedures were randomly assigned to groups.

Reporting Groups

	Description
Behavioral Skills Training	Multicomponent behavioral intervention using 10-session video series (Steffen, et al., 2001) workbook (Steffen, et al., 2001), and weekly telephone coaching sessions.
Basic Education	Participants receive 37-page Basic Care Guide (Education Institute, 2001) and bi-weekly telephone calls by a trained staff member.

Participant Flow: Overall Study

	Behavioral Skills Training	Basic Education
STARTED	33	41^[1]
COMPLETED	30	38
NOT COMPLETED	3	3
Withdrawal by Subject	2	2
Death/NH placement of pt	1	1

[1]	over-enrolled due to potential higher rates of drop-out.

Baseline Characteristics

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Outcome Measures

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1. Primary:

Beck Depression Inventory II (Beck, Steer & Brown, 1996) [ Pre-intervention intake assessment, conducted 7-14 days prior to start of intervention ]

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2. Primary:

Primary Outcome: Beck Depression Inventory II (Beck, Steer & Brown, 1996) [ Post-intervention, assessed 4-14 days after final intervention session. ]

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3. Secondary:

Negative Affect Schedule (Watson, Clark & Tellegen, 1988) [ Pre-intervention intake assessment, conducted 7-14 days prior to start of intervention ]

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4. Secondary:

Secondary Outcome: Negative Affect Scale (Watson, Clark & Tellegen, 1988) [ Post-intervention, assessed 4-14 days after final intervention session. ]

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Serious Adverse Events

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Other Adverse Events

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More Information

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Certain Agreements:

Principal Investigators are NOT employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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Results Point of Contact:

Name/Title: Ann M. Steffen, PhD, Associate Professor
Organization: University of Missouri-St. Louis
phone: 314-516-5382
e-mail: ann_steffen@umsl.edu

Publications:

Steffen AM. Anger management for dementia caregivers: A preliminary study using video and telephone interventions. Behavior Therapy 31:281-299, 2000.

Steffen AM, McKibbin C, Zeiss AM, Gallagher-Thompson D, Bandura A. The revised scale for caregiving self-efficacy: reliability and validity studies. J Gerontol B Psychol Sci Soc Sci. 2002 Jan;57(1):P74-86.

Responsible Party:	University of Missouri-St. Louis ( Ann M. Steffen, Ph.D./Associate Professor of Psychology )
Study ID Numbers:	R21 MH61956, DSIR AT-GS
Study First Received:	March 10, 2003
Results First Received:	October 23, 2008
Last Updated:	November 17, 2008
ClinicalTrials.gov Identifier:	NCT00056316 History of Changes
Health Authority:	United States: Federal Government