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Cognitive Behavioral Therapy for Insomnia: Face-to-Face Versus Telemedicine

Primary Purpose

Insomnia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Face to Face CBT-I (F2F)
Telemedicine CBT-I (TM)
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

1. Current diagnosis of insomnia

Exclusion Criteria:

  1. Suspicion of or inadequately treated sleep disorder other than insomnia
  2. Presence of psychiatric disorders for which CBT for insomnia may be contraindicated
  3. Unstable chronic medical condition directly related to insomnia
  4. Routine overnight shift work
  5. Previous failed adequate trial of CBT for insomnia
  6. Unstable dose of sleep medications
  7. Lack of access to reliable WiFi connection in the home

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Face to Face CBT-I (F2F)

Telemedicine CBT-I (TM)

Arm Description

Participants in the F2F arm will receive a standard 6-session course of Cognitive-Behavioral Therapy for Insomnia (CBT-I) delivered in-person, one-on-one with a qualified and experienced therapist.

Participants in the F2F arm will receive a standard 6-session course of Cognitive-Behavioral Therapy for Insomnia (CBT-I) delivered via the American Academy of Sleep Medicine (AASM) Sleep Telemedicine system. This telemedicine system provides an online videoconference platform in which a qualified and experienced therapist will deliver CBT-I to participants who will call in to the video therapy sessions with their provider from their homes using a webcam. All aspects of the treatment will remain identical to standard CBT-I delivered face-to-face, as described above, with the exception that the telemedicine technology will be used to deliver the treatment via video conference.

Outcomes

Primary Outcome Measures

Change in Insomnia Severity Index (ISI)
The ISI is a 7-item questionnaire assessing the nature, severity, and impact of sleep problems, with good psychometric properties and sensitivity to change with treatment 0-7 = No clinically significant insomnia 8-14 = Subthreshold insomnia 15-21 = Clinical insomnia (moderate severity) 22-28 = Clinical insomnia (severe)

Secondary Outcome Measures

Client Satisfaction Questionnaire (CSQ-8)
The CSQ-8 is an 8-item, easily scored and administered measurement that is designed to measure client satisfaction with services. The items for the CSQ-8 were selected on the basis of ratings by mental health professionals of a number of items that could be related to client satisfaction and by subsequent factor analysis. The CSQ-8 is unidimensional, yielding a homogeneous estimate of general satisfaction with services. Scores range from 8 - 32, with high scores indicating greater satisfaction.
Change in Therapy Evaluation Questionnaire (TEQ)
The TEQ is a 7-item scale with 5 questions to assess perceived logic of and confidence in treatment, willingness to repeat treatment, and the likelihood that the treatment will help others and 2 questions assessing therapist warmth and competence.

Full Information

First Posted
September 19, 2017
Last Updated
January 25, 2023
Sponsor
University of Michigan
Collaborators
American Academy of Sleep Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT03293745
Brief Title
Cognitive Behavioral Therapy for Insomnia: Face-to-Face Versus Telemedicine
Official Title
Cognitive Behavioral Therapy for Insomnia: Face-to-Face Versus Telemedicine
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
November 15, 2017 (Actual)
Primary Completion Date
October 4, 2019 (Actual)
Study Completion Date
October 4, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
American Academy of Sleep Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of this study is to compare the effectiveness of Cognitive-Behavioral Therapy (CBT) for insomnia conducted face-to-face with a therapist versus CBT for insomnia conducted using Internet-based videoconference technology.
Detailed Description
The objective of this clinical trial is to compare the effectiveness of telemedicine Cognitive-Behavioral Therapy (CBT) for insomnia [via the American Academy of Sleep Medicine Sleep Telemedicine (AASM Sleep TM) platform] to gold standard face-to-face CBT for insomnia. The central hypothesis is that CBT for insomnia delivered by AASM SleepTM will be comparable to face-to-face CBT for insomnia for clinical outcomes and patient satisfaction, but AASM SleepTM will be a more cost effective treatment modality (primarily through reduced costs associated with facility use and patient time). The rationale for the proposed project is rooted in the critical need to disseminate CBT for insomnia using the most effective and efficient modalities, with recognition that therapist involvement likely produces the most favorable outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
65 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Face to Face CBT-I (F2F)
Arm Type
Active Comparator
Arm Description
Participants in the F2F arm will receive a standard 6-session course of Cognitive-Behavioral Therapy for Insomnia (CBT-I) delivered in-person, one-on-one with a qualified and experienced therapist.
Arm Title
Telemedicine CBT-I (TM)
Arm Type
Experimental
Arm Description
Participants in the F2F arm will receive a standard 6-session course of Cognitive-Behavioral Therapy for Insomnia (CBT-I) delivered via the American Academy of Sleep Medicine (AASM) Sleep Telemedicine system. This telemedicine system provides an online videoconference platform in which a qualified and experienced therapist will deliver CBT-I to participants who will call in to the video therapy sessions with their provider from their homes using a webcam. All aspects of the treatment will remain identical to standard CBT-I delivered face-to-face, as described above, with the exception that the telemedicine technology will be used to deliver the treatment via video conference.
Intervention Type
Behavioral
Intervention Name(s)
Face to Face CBT-I (F2F)
Intervention Description
CBT-I delivered in-person by the therapist.
Intervention Type
Behavioral
Intervention Name(s)
Telemedicine CBT-I (TM)
Intervention Description
CBT-I delivered via American Academy of Sleep Medicine Telemedicine video conference System by the therapist.
Primary Outcome Measure Information:
Title
Change in Insomnia Severity Index (ISI)
Description
The ISI is a 7-item questionnaire assessing the nature, severity, and impact of sleep problems, with good psychometric properties and sensitivity to change with treatment 0-7 = No clinically significant insomnia 8-14 = Subthreshold insomnia 15-21 = Clinical insomnia (moderate severity) 22-28 = Clinical insomnia (severe)
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Secondary Outcome Measure Information:
Title
Client Satisfaction Questionnaire (CSQ-8)
Description
The CSQ-8 is an 8-item, easily scored and administered measurement that is designed to measure client satisfaction with services. The items for the CSQ-8 were selected on the basis of ratings by mental health professionals of a number of items that could be related to client satisfaction and by subsequent factor analysis. The CSQ-8 is unidimensional, yielding a homogeneous estimate of general satisfaction with services. Scores range from 8 - 32, with high scores indicating greater satisfaction.
Time Frame
Post-treatment (about 6 weeks)
Title
Change in Therapy Evaluation Questionnaire (TEQ)
Description
The TEQ is a 7-item scale with 5 questions to assess perceived logic of and confidence in treatment, willingness to repeat treatment, and the likelihood that the treatment will help others and 2 questions assessing therapist warmth and competence.
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Other Pre-specified Outcome Measures:
Title
Change in Patient Health Questionnaire - 9 (PHQ-9).
Description
The PHQ-9 is a 9-item scale measuring the severity of depressive symptoms (range = 0 - 27, with higher scores reflecting more severe depression).
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in Generalized Anxiety Disorder Questionnaire - 7 (GAD-7)
Description
The GAD-7 is a 7-item survey that measures the severity of anxiety symptoms (range = 0-21, with higher scores reflecting higher levels of anxiety).
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in Short-Form Health Survey (SF-12)
Description
The 12-item Short-Form Health Survey (SF-12) is a short-form quality of life measure derived from the Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36), which computes physical and mental composite scale scores ranging from 0 to 100.
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in Multidimensional Fatigue Inventory (MFI-20)
Description
The MFI-20 is a 20-item scale with five subscales representing dimensions of general fatigue, physical fatigue, mental fatigue, reduced motivation, and reduced activity. Higher scores indicate greater fatigue.
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in Dysfunctional Beliefs About Sleep Scale (DBAS).
Description
The DBAS is a 16-item measure (range: 0-160, with greater scores reflection greater degrees of negative thinking and beliefs related to sleep which presents a series of negative statements or beliefs about sleep. Patients rate the degree to which they agree with or believe each statement.
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in Work and Social Adjustment Scale (WSAS).
Description
The WSAS is a 5-item questionnaire assessing perceived degree of impairment in work and social domains. Scores range from 0 to 40, with higher scores reflecting greater levels of impairment.
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in Cornell Service Utilization Index (CSUI).
Description
The CSUI is a 10-item measure that assesses participants' use of medical and mental health services over a six month period.
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in Working Alliance Inventory - Short Revised (WAI-SR).
Description
The WAI-SR is a 12-item measure that assesses the degree to which patients perceive a positive working relationship with their therapist. Scores range from 12-60, with higher scores reflecting greater levels of perceived working alliance with the therapist.
Time Frame
Weekly for about 6 weeks
Title
Change in sleep diary measures
Description
Participants will keep sleep diaries daily for 2 weeks at baseline, during treatment, for 2 weeks post-treatment, and for 2 weeks at 12-week post-treatment follow-up. Primary outcomes will include mean sleep efficiency (SE = total sleep time/time in bed*100)
Time Frame
Baseline, daily during the 6-week treatment, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)
Title
Change in actigraphy measures
Description
Participants will wear an actigraph for 2 weeks at baseline, for 2 weeks post-treatment and for 2 weeks at 12-week post-treatment follow-up. Outcomes will include mean sleep efficiency (SE = total sleep time/time in bed*100)
Time Frame
Baseline, post-treatment (about 6 weeks), follow-up (about 12-weeks post-treatment)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. Current diagnosis of insomnia Exclusion Criteria: Suspicion of or inadequately treated sleep disorder other than insomnia Presence of psychiatric disorders for which CBT for insomnia may be contraindicated Unstable chronic medical condition directly related to insomnia Routine overnight shift work Previous failed adequate trial of CBT for insomnia Unstable dose of sleep medications Lack of access to reliable WiFi connection in the home
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Todd Arnedt, PhD
Organizational Affiliation
University of Michigan Department of Psychiatry
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
32658298
Citation
Arnedt JT, Conroy DA, Mooney A, Furgal A, Sen A, Eisenberg D. Telemedicine versus face-to-face delivery of cognitive behavioral therapy for insomnia: a randomized controlled noninferiority trial. Sleep. 2021 Jan 21;44(1):zsaa136. doi: 10.1093/sleep/zsaa136.
Results Reference
derived

Learn more about this trial

Cognitive Behavioral Therapy for Insomnia: Face-to-Face Versus Telemedicine

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