Feasibility of Telehealth Problem-Solving Therapy for Depressed Homebound Older Adults

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2012 by University of Texas at Austin.
Recruitment status was  Active, not recruiting
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Namkee Choi, University of Texas at Austin
ClinicalTrials.gov Identifier:
NCT00903019
First received: May 13, 2009
Last updated: April 23, 2012
Last verified: April 2012
  Purpose

This study will test the feasibility and effectiveness of therapy given via teleconferencing to depressed homebound older adults.


Condition Intervention
Depression
Behavioral: Tele-Problem-Solving Therapy
Behavioral: In-Person PST
Behavioral: Attention control

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Health Services Research
Official Title: Telehealth Problem-Solving Therapy for Depressed Homebound Older Adults

Resource links provided by NLM:


Further study details as provided by University of Texas at Austin:

Primary Outcome Measures:
  • 24-item Hamilton Rating Scale for Depression (HAMD) [ Time Frame: Measured at 2, 12, and 24 weeks ] [ Designated as safety issue: No ]
  • 12-item World Health Organization Disability Assessment Schedule (WHO-DAS-II) [ Time Frame: Measured at 2, 12, and 24 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 100
Study Start Date: June 2009
Estimated Study Completion Date: August 2012
Estimated Primary Completion Date: August 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
Participants will receive problem-solving therapy (PST) delivered via teleconferencing (tele-PST).
Behavioral: Tele-Problem-Solving Therapy
Six sessions of tele-PST
Active Comparator: 2
Participants will receive problem-solving therapy (PST) delivered in-person.
Behavioral: In-Person PST
Six sessions of in person PST
Placebo Comparator: 3
Participants will receive monitoring phone calls.
Behavioral: Attention control
Six weekly telephone calls

Detailed Description:

Older people with disabilities who cannot leave their homes are at increased risk of depression or depressive symptoms. Short-term psychotherapy, without medications, has been found effective for treating this population of people. Problem-solving therapy (PST) is a brief, structured, cognitive-behavioral therapy that teaches people problem-solving and coping skills to deal with negative life events and daily problems. Previous research demonstrated that PST is an effective treatment for depression when delivered to older adults in their homes. The cost of service for these in-home visits, however, can be prohibitive for many older adults and social service providers. One way to extend treatment to more older adults is to deliver PST via teleconferencing (tele-PST). This study will test the feasibility and effectiveness of tele-PST in treating depression in homebound older adults.

This study will have two phases. Phase 1 will examine the feasibility of delivering treatment via teleconference. Participants in this phase will receive six weekly sessions of tele-PST and then complete a 2-week follow-up visit in which their depression, disability, and resourcefulness will be assessed. Logistical and procedural problems and acceptability of the treatment to participants will be used to guide modifications or adaptations made to tele-PST before conducting a larger, randomized trial in Phase 2.

Participation in Phase 2 will last 6 weeks, with follow-up visits lasting until 24 weeks after the conclusion of treatment. Participants will be randomly assigned to one of three groups: tele-PST, in-person PST, and attention control. Participants in the tele-PST group will receive six weekly sessions of PST via teleconference, and participants in the in-person PST group will receive six weekly sessions of PST from a study therapist in person. Both these groups will also receive six monthly maintenance calls from their study therapist after the completion of treatment. Participants in the attention group will receive six weekly phone calls followed by six monthly phone calls to monitor their health. All participants in Phase 2 will complete assessments at 2, 12, and 24 weeks following their treatment. These assessments will measure the adequacy of recruitment, enrollment, and retention strategies; the compliance rates and service delivery costs of tele-PST and in-person PST; and participants' depression, disability, and resourcefulness.

  Eligibility

Ages Eligible for Study:   50 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Non-Hispanic white, African American, or Hispanic
  • Homebound, as defined by receiving a home-delivered meals service or personal assistance and in-home support services because of disability
  • Moderate-to-severe depressive symptom severity, as defined by a score greater than or equal to 15 on the Hamilton Rating Scale for Depression (HAMD)
  • Has a home television set that can be used for problem-solving therapy (PST) sessions
  • Has a landline telephone

Exclusion Criteria:

  • High suicide risk, as defined by an intent or plan to attempt suicide within a month or indication of persistently moderate or severe suicidal ideation or behavior
  • Presence of dementia or executive dysfunction
  • Presence of bipolar disorder
  • Lifetime or current (within 12 months) psychotic symptoms or disorder
  • Presence of co-occurring alcohol or other addictive substance abuse, including benzodiazepines and opioids
  • Hearing or vision impairment that would interfere with PST participation
  • Inability to actively participate in PST sessions due to acute or severe medical illness or functional impairment, such as a bed-bound state
  • Current involvement in psychotherapy
  • Inability to speak English
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00903019

Locations
United States, Texas
University of Texas at Austin
Austin, Texas, United States, 78712-0358
Sponsors and Collaborators
University of Texas at Austin
Investigators
Principal Investigator: Namkee G. Choi, PhD University of Texas at Austin
  More Information

No publications provided by University of Texas at Austin

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Namkee Choi, Professor, University of Texas at Austin
ClinicalTrials.gov Identifier: NCT00903019     History of Changes
Other Study ID Numbers: R34 MH083872, R34MH083872, DATR A4-GPS
Study First Received: May 13, 2009
Last Updated: April 23, 2012
Health Authority: United States: Federal Government

Keywords provided by University of Texas at Austin:
Homebound
Older Adults
Disability
Videoconferencing

Additional relevant MeSH terms:
Depression
Depressive Disorder
Behavioral Symptoms
Mood Disorders
Mental Disorders

ClinicalTrials.gov processed this record on April 17, 2014