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Interactive CBT for Headache And Relaxation Training (iCHART)

Primary Purpose

Post-Traumatic Headache

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
iCHART - Interactive CBT for Headache And Relaxation Training
Sponsored by
VA Connecticut Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-Traumatic Headache

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of post-traumatic headache disorder (migraine and/or tension-type subtype)
  • Frequency of ≥4 headache days per month
  • Primary pain complaint of headache
  • Access to a touchtone telephone and computer/tablet

Exclusion Criteria:

  • Non-English speaking
  • Non-Veteran
  • Receiving hospice or palliative care
  • Sensory deficits that would impair participation in the IVR telephone calls
  • Significant cognitive impairment
  • Inpatient psychiatric hospitalization for any psychiatric or substance use diagnosis in the past 30 days from screening
  • Active psychotic symptoms, suicidality, or severe depressive symptoms
  • Suicidal and/or homicidal ideation in the past 6 months from screening

Sites / Locations

  • VACHSRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

iCHART - Interactive CBT for Headache And Relaxation Training

Arm Description

10 week interactive-voice response technology (IVR) based cognitive behavioral therapy for headache

Outcomes

Primary Outcome Measures

Change in headache days
Daily self-reported headache days

Secondary Outcome Measures

Change in headache-related disability
Headache Disability Inventory (HDI) is a 25-item self-report questionnaire that assesses both emotional and functional impact of headache on daily activities. Item response options include "yes", "sometimes", and "no." Total scores range from 0 to 100. Higher scores indicate higher levels of reported disability.
Change in headache-related disability
Migraine Disability Assessment (MIDAS) is a 5-item, self-report measure of life disruption due to headache. Cut points represent thresholds for little or no disability (0-5), mild disability (6-10), moderate disability (11-20), and severe disability (21+).

Full Information

First Posted
September 22, 2021
Last Updated
June 23, 2022
Sponsor
VA Connecticut Healthcare System
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1. Study Identification

Unique Protocol Identification Number
NCT05093556
Brief Title
Interactive CBT for Headache And Relaxation Training
Acronym
iCHART
Official Title
Interactive CBT for Headache And Relaxation Training (iCHART)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 6, 2022 (Actual)
Primary Completion Date
October 20, 2022 (Anticipated)
Study Completion Date
February 20, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Connecticut Healthcare System

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This mixed-methods pilot study aims to evaluate the feasibility, acceptability, and preliminary effectiveness of iCHART (Interactive CBT for Headache And Relaxation Training), an interactive voice response (IVR) based delivery of cognitive behavioral therapy for Veterans with post-traumatic headache. Participants will receive iCHART treatment through the IVR system over a period of 10 weeks, which will include an automated daily assessment of patient-reported outcomes, retrieval of fortnightly tailored feedback from a study therapist, and additional weekly one-way motivational enhancement messaging. Delivery of traditional evidence-based behavioral treatments for headache management through technology-based interventions, such as IVR may ultimately increase much needed access to these treatments and allow patients to receive care at a time that is convenient for them.
Detailed Description
Headache disorders are prevalent and highly disabling chronic neurological pain conditions, especially among women and people with traumatic brain injury, yet remain underdiagnosed and undertreated. Cognitive behavioral therapy for headache is an evidence-based psychological treatment that is effective in reducing headache frequency and severity, addressing psychiatric comorbidities, and improving an individual's quality of life, yet it remains hugely underutilized and inaccessible to many. Delivery of traditional evidence-based behavioral treatments for headache management through technology-based interventions may ultimately increase much needed access to these treatments. Interactive voice response (IVR) is an automated telephone-based technology where people receive tailored messaging which allows them to track symptoms, target behavior change, and engage in disease self-management. This mixed-methods pilot study aims to evaluate the feasibility, acceptability, and preliminary effectiveness of iCHART (Interactive CBT for Headache And Relaxation Training), an IVR-based delivery of cognitive behavioral therapy for Veterans with headache. Participants will be thirty-five Veterans receiving care within VA Connecticut Healthcare System, who are diagnosed with post-traumatic headache. All eligible participants will complete an initial intake interview and a 28-day electronic headache diary. Following the baseline assessment period, eligible participants will then receive iCHART treatment through the IVR system over a period of 10 weeks, which will include an automated daily assessment of patient-reported outcomes, retrieval of fortnightly tailored feedback from a study therapist, and additional weekly one-way motivational enhancement messaging. Participants will access a patient workbook via the iCHART study website and iCHART providers will visualize patient-reported data through the secure iCHART provider dashboard. Assessment measures will be completed at baseline, immediately post-treatment completion, and one month post-treatment completion. Analysis of primary and secondary outcome measures will employ mixed methods.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-Traumatic Headache

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
35 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
iCHART - Interactive CBT for Headache And Relaxation Training
Arm Type
Experimental
Arm Description
10 week interactive-voice response technology (IVR) based cognitive behavioral therapy for headache
Intervention Type
Behavioral
Intervention Name(s)
iCHART - Interactive CBT for Headache And Relaxation Training
Intervention Description
IVR based cognitive behavioral therapy for headache
Primary Outcome Measure Information:
Title
Change in headache days
Description
Daily self-reported headache days
Time Frame
Baseline and week 14
Secondary Outcome Measure Information:
Title
Change in headache-related disability
Description
Headache Disability Inventory (HDI) is a 25-item self-report questionnaire that assesses both emotional and functional impact of headache on daily activities. Item response options include "yes", "sometimes", and "no." Total scores range from 0 to 100. Higher scores indicate higher levels of reported disability.
Time Frame
Baseline and week 14
Title
Change in headache-related disability
Description
Migraine Disability Assessment (MIDAS) is a 5-item, self-report measure of life disruption due to headache. Cut points represent thresholds for little or no disability (0-5), mild disability (6-10), moderate disability (11-20), and severe disability (21+).
Time Frame
Baseline and week 14
Other Pre-specified Outcome Measures:
Title
Veterans RAND 12-item Health Survey (VR-12)
Description
A 12-item, self-report measure of health-related quality life in terms of physical and mental health domains. Scores are summed into a physical health and mental health summary score and standardized using a T-score metric with a mean of 50 and a standard deviation of 10.
Time Frame
Baseline, week 10, and week 14
Title
Patient Health Questionnaire 8-item (PHQ-8)
Description
An 8-item, self-report measure of depressive symptom severity based on DSM criteria. Items are rated from 0 to 3 (0 = not at all to 3 = nearly every day). Total scores range from 0 to 27. Cut points represent thresholds for non-minimal (0-4), mild (5-9), moderate (10-14), moderately severe (15-19), and severe (20-27) depression.
Time Frame
Baseline, week 10, and week 14
Title
Generalized Anxiety Disorder Screener (GAD-7)
Description
A 7-item, self-report measure of anxiety. Items are rated from 0 to 3 (0 = not at all to 3 = nearly every day). Total scores range from 0 to 21. Cut points represent thresholds for none-minimal (0-4), mild (5-9), moderate (10-14) and severe (15-21).
Time Frame
Baseline, week 10, and week 14
Title
Post-Traumatic Stress Disorder Checklist (PCL)
Description
A 17-tem, self-report measure of symptoms of PTSD based on Diagnostic and Statistical Manual (DSM) criteria. Items are rated from 0 to 4 (0= Not at all to 4 = Extremely). Total scores range from 17-85.
Time Frame
Baseline, week 10, and week 14
Title
Insomnia Severity Index (ISI)
Description
A 5-item self-report measure of symptoms of insomnia. Total scores range from 0 to 28. Cut points represent thresholds for no clinically significant insomnia (0-7), subthreshold insomnia (8-14), clinical insomnia (moderately severe) (15-21), clinical insomnia (severe) (22-28).
Time Frame
Baseline, week 10, and week 14
Title
Headache Pain Catastrophizing Scale (HPCS)
Description
A modified version of the Pain Catastrophizing Scale (use of word headache vs. pain in the questions). The HPCS is a 13-item self-report measure of catastrophic thinking related to headache. Items are rated from 0 to 4 (0= not at all to 4 - all the time). Total scores range from 0 to 52, with subscale scores for rumination, magnification, and helplessness.
Time Frame
Baseline, week 10, and week 14
Title
Headache Management Self-Efficacy Scale (HMSE)
Description
A 25-item self-report questionnaire related to a person's confidence in their ability to manage their headache symptoms. Items range from 1 to 7 (1=strongly disagree to 7 = strongly disagree). Total scores range from 25 to 175
Time Frame
Baseline, week 10, and week 14
Title
Patient Global Perception of Change (PGPC)
Description
single item scale measures the participant's perception of improvement since the start of the study. Participants respond to the single item on a 7-point scale (1 = very much improved to 7 = very much worse). This measure shows good psychometric properties.
Time Frame
Week 10
Title
Client Satisfaction Questionnaire-8 (CSQ-8)
Description
An 8-item self-report measure of treatment acceptability and satisfaction with mental health treatment. Items are coded on a 4-point scale. Total scores are calculated by summing up items, with scores ranging from 8 to 32
Time Frame
Week 10
Title
System Usability Scale (SUS)
Description
A 10-item measure of treatment acceptability. The SUS assesses participant perceived usability of technology systems. Response options range from 1 to 5, with 50% of the items being positively worded and 50% negatively worded. Scores are converted to an overall score from 0 to 100. Higher scores indicate higher perceived usability
Time Frame
Week 10
Title
Acceptability of Intervention (AIM)
Description
A 4-item measure of treatment acceptability. Items are score on a 5-point scale. Scores are a calculated mean. Higher scores indicate greater acceptability
Time Frame
Week 10
Title
Structured Assessment of Feasibility Questionnaire (SAFE)
Description
A 16-item measure of feasibility of mental health services, organized into two sections. The first eight questions assess barriers to implementation, the final eight assess facilitators to implementation. Items are rated as either yes, partial, no, or unable to rate, with each individual item attended to. It is recommended against using a summary score, since items within the sale may have unequal weight.
Time Frame
Week 10
Title
Feasibility of Intervention Measure (FIM)
Description
A 4-item measure of feasibility. Items are rated on a 5-point Likert scale. Scores are a calculated mean. Higher scores indicate greater feasibility
Time Frame
Week 10

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of post-traumatic headache disorder (migraine and/or tension-type subtype) Frequency of ≥4 headache days per month Primary pain complaint of headache Access to a touchtone telephone and computer/tablet Exclusion Criteria: Non-English speaking Non-Veteran Receiving hospice or palliative care Sensory deficits that would impair participation in the IVR telephone calls Significant cognitive impairment Inpatient psychiatric hospitalization for any psychiatric or substance use diagnosis in the past 30 days from screening Active psychotic symptoms, suicidality, or severe depressive symptoms Suicidal and/or homicidal ideation in the past 6 months from screening
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amy Grinberg, PhD
Phone
203-932-5711
Email
amy.grinberg@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amy Grinberg, PhD
Organizational Affiliation
VA Connecticut Healthcare System
Official's Role
Principal Investigator
Facility Information:
Facility Name
VACHS
City
West Haven
State/Province
Connecticut
ZIP/Postal Code
06516
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amy Grinberg, PhD
Phone
203-932-5711
Email
amy.grinberg@va.gov

12. IPD Sharing Statement

Learn more about this trial

Interactive CBT for Headache And Relaxation Training

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