- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01906476
Stepped Telemental Health Care Intervention for Depression
February 6, 2023 updated by: David Mohr, Northwestern University
This is a randomized, controlled trial comparing telephone-cognitive behavior therapy (T-CBT) with a therapist to a "Stepped Care" intervention for depression treatment (iCBT with support from a telephone coach with the possibility of being stepped up to receiving T-CBT with a therapist).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Major depressive disorder (MDD) is common, with 12-month prevalence rates estimated to be between 6.6-10.3%.
While many depressed patients state they would prefer psychological treatment to pharmacotherapy, substantial barriers to care exist, including cost, practical barriers such as time constraints and transportation, emotional barriers such as stigma, decreased motivation associated with depression itself, physical disability, and lack of availability of services.
Telemental health has been proposed as a method of overcoming barriers to treatment.
Research has focused primarily on two formats: the telephone and the Internet.
Use of the telephone as a delivery medium produces reductions in depression equivalent to face-to-face psychological treatments, while also significantly reducing attrition.
However, its success in outreach can also significantly increase costs for healthcare providing organizations.
Internet interventions have the potential to produce moderate gains when supported by therapist or coach via brief telephone calls or e-mail but are also less expensive than standard therapy.
Developing healthcare models that integrate treatment delivery media holds the promise of harnessing the advantages of each media, while minimizing the disadvantages.
Stepped care models are a potentially useful framework for achieving such an integration.
The stepped care model we will test initiates treatment with a validated, guided Internet cognitive behavioral therapy program.
If patients fail to respond, they will be stepped up to a validated telephone-cognitive behavior therapy (T-CBT).
The stepped care model will be compared to T-CBT in a randomized trial.
Patients will be recruited from primary care and treated for up to 20 weeks, or until sustained remission is achieved.
Study Type
Interventional
Enrollment (Actual)
312
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60611
- Northwestern University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Has a DSM-IV diagnosis of non-psychotic major depressive disorder (MDD) as assessed using the Mini International Neuropsychiatric Interview (MINI), plus a score of 12 or greater on the Quick Inventory of Depressive Symptomatology - Clinician Rated (QIDS-C)
- Has a phone, access to the Internet, and basic internet skills
- Is at least 18 years of age
- Is able to speak and read English
- If currently taking an antidepressant medication, participant must have been on a stable dose for at least two weeks, and have no plans to change the dose
Exclusion Criteria:
- Has visual, hearing, voice, or motor impairment that would prevent completion of study procedures
- Is diagnosed with a psychotic disorder, bipolar disorder, dissociative disorder, substance use or other diagnosis for which participation in this trial is either inappropriate or dangerous
- Is severely suicidal (has ideation, plan, and intent)
- Is currently receiving or planning to begin psychotherapy during the study treatment period
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Stepped Care
Participants will receive an Internet guided cognitive behavioral treatment (iCBT) with support from a telephone coach with the possibility of being stepped up to receiving telephone cognitive behavior therapy (T-CBT) with a therapist
|
Participants will receive an Internet guided cognitive behavioral treatment (iCBT) with support from a telephone coach with the possibility of being stepped up to receiving telephone cognitive behavior therapy (T-CBT) with a therapist
|
|
ACTIVE_COMPARATOR: Telephone Cognitive Behavior Therapy
Participants will receive telephone-administered cognitive behavioral therapy (T-CBT).
|
Participants will receive telephone-administered cognitive behavioral therapy (T-CBT).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Depression
Time Frame: Baseline, midtreatment, end of treatment, 3 month post treatment, and 6 month post-treatment follow-up
|
To measure changes in the Quick Inventory of Depressive Symptomatology (QIDS) over time.
The QIDS is made up of 16 items and has a possible range of scores of 0 to 27.
Higher scores represent worse outcomes.
|
Baseline, midtreatment, end of treatment, 3 month post treatment, and 6 month post-treatment follow-up
|
|
Cost-Effectiveness
Time Frame: Baseline to end of treatment
|
Measure the ratio of the difference in costs and difference in effectiveness between the two groups, Stepped care minus Telephone Cognitive Behavior Therapy.
Below are reported individual cost means and standard deviations for therapist costs during study.
|
Baseline to end of treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
February 1, 2015
Primary Completion (ACTUAL)
April 1, 2018
Study Completion (ACTUAL)
April 1, 2018
Study Registration Dates
First Submitted
July 17, 2013
First Submitted That Met QC Criteria
July 19, 2013
First Posted (ESTIMATE)
July 24, 2013
Study Record Updates
Last Update Posted (ACTUAL)
February 8, 2023
Last Update Submitted That Met QC Criteria
February 6, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01MH095753-01A1-RCTTH
- R01MH095753-01A1 (NIH)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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