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

NCT ID: NCT00903019

Last Updated: 2015-03-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

158 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-06-30

Study Completion Date

2013-05-31

Brief Summary

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

Detailed Description

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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.

Conditions

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Depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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1

Participants will receive problem-solving therapy (PST) delivered via teleconferencing (tele-PST).

Group Type EXPERIMENTAL

Tele-Problem-Solving Therapy

Intervention Type BEHAVIORAL

Six sessions of tele-PST

2

Participants will receive problem-solving therapy (PST) delivered in-person.

Group Type ACTIVE_COMPARATOR

In-Person PST

Intervention Type BEHAVIORAL

Six sessions of in person PST

3

Participants will receive monitoring phone calls.

Group Type PLACEBO_COMPARATOR

Attention control

Intervention Type BEHAVIORAL

Six weekly telephone calls

Interventions

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Tele-Problem-Solving Therapy

Six sessions of tele-PST

Intervention Type BEHAVIORAL

In-Person PST

Six sessions of in person PST

Intervention Type BEHAVIORAL

Attention control

Six weekly telephone calls

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

University of Texas at Austin

OTHER

Sponsor Role lead

Responsible Party

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Namkee Choi

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Namkee G. Choi, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Texas at Austin

Locations

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University of Texas at Austin

Austin, Texas, United States

Site Status

Countries

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United States

References

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Choi NG, Marti CN, Bruce ML, Kunik ME. Relationship between depressive symptom severity and emergency department use among low-income, depressed homebound older adults aged 50 years and older. BMC Psychiatry. 2012 Dec 26;12:233. doi: 10.1186/1471-244X-12-233.

Reference Type DERIVED
PMID: 23267529 (View on PubMed)

Other Identifiers

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R34MH083872

Identifier Type: NIH

Identifier Source: secondary_id

View Link

DATR A4-GPS

Identifier Type: -

Identifier Source: secondary_id

R34MH083872

Identifier Type: NIH

Identifier Source: org_study_id

View Link

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