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Study Results
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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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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.

Baseline Measures
  Behavioral Skills Training Basic Education Total
Number of Participants  
[units: participants]
33 41 74
Age  
[units: participants]
     
<=18 years 0 0 0
Between 18 and 65 years 23 26 49
>=65 years 10 15 25
Age  
[units: years]
Mean ± Standard Deviation
58.4 ± 11.9 62.9 ± 9.6 61.1 ± 11.1
Gender  
[units: participants]
     
Female 33 41 74
Male 0 0 0
Region of Enrollment  
[units: participants]
     
United States 33 41 74



  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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Measure Type Primary
Measure Title Beck Depression Inventory II (Beck, Steer & Brown, 1996)
Measure Description 21-item self-report instrument to assess severity of symptoms of depression. There is a four-point scale for each item ranging from 0 to 3. The total continuous score can range from 0 to 63 points, with higher scores reflective of greater severity.
Time Frame Pre-intervention intake assessment, conducted 7-14 days prior to start of intervention  
Safety Issue No  

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
all randomized participants

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.

Measured Values
  Behavioral Skills Training Basic Education
Number of Participants Analyzed
[units: participants]
33 41
Beck Depression Inventory II (Beck, Steer & Brown, 1996)
[units: points on a scale]
Mean ± Standard Deviation
14.27 ± 8.07 16.93 ± 8.46

No statistical analysis provided for Beck Depression Inventory II (Beck, Steer & Brown, 1996)



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

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

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


  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
No text entered.  


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