N/A
N=87
Telemedicine Management of Chronic Insomnia
Sleep Initiation and Maintenance Disorders · Post-Traumatic Stress Disorders
Bottom Line
View on ClinicalTrials.gov: NCT01686438 ↗Enrolled (actual)
87
Serious AEs
1.2%
Results posted
Aug 2019
Primary outcome: Primary: Change From Baseline in Insomnia Severity Index Score — 6.68; 5.13 units on a scale — p=0.138
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Cognitive behavioral therapy for insomnia (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- VA Office of Research and Development
- Primary completion
- Nov 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in Insomnia Severity Index Score |
6.68; 5.13 | 0.138 |
| SECONDARY Change From Baseline PTSD Checklist-Military (PCL-M) Scores |
3.30; 5.73; 5.22 | — |
| SECONDARY Change From Baseline Pittsburgh Sleep Quality Index (PSQI) Scores |
2.03; 3.34; 2.50 | — |
| SECONDARY Change From Baseline in Pittsburgh Sleep Quality Index Addendum for PTSD (PSQI-A) |
0.30; 0.23; 0.51 | — |
| SECONDARY Change From Baseline in Nightmare Distress Questionnaire Scores |
-3.78; -2.65; -0.11 | — |
| SECONDARY Change From Baseline Medical Outcomes Study Short Form-12 (SF-12) Mental Component Score |
0.26; 0.70; 2.76 | — |
| SECONDARY Change From Baseline in Medical Outcomes Study Short Form-12 (SF-12) Physical Component Score |
3.31; -1.37; 0.14 | — |
| SECONDARY Change From Baseline in Work and Social Adjustment Scale Scores |
-0.54; 0.01; -0.85 | — |
| SECONDARY Working Alliance Inventory - Short Revised (WAI-SR) - Task Formation Scores at 8 Weeks |
62.5; 76.8; 74.1 | — |
| SECONDARY Charleston Psychiatric Outpatient Satisfaction Scale-VA Scores at 8 Weeks |
47.5; 46.7; 44.8 | — |
| SECONDARY Change From Baseline in Nightmare Frequency Questionnaire (NFQ) Part 1 Scores |
-26.1; 11.35; -3.04 | — |
| SECONDARY Change From Baseline in Nightmare Frequency Questionnaire (NFQ) Part 2 Scores |
-24.6; 6.41; -8.09 | — |
| SECONDARY Working Alliance Inventory - Short Revised (WAI-SR) - Bond Formation at 8 Weeks |
72.8; 77.4; 76.8 | — |
| SECONDARY Working Alliance Inventory - Short Revised (WAI-SR) - Goal Formation at 8 Weeks |
67.5; 75.8; 75.3 | — |
Summary
Insomnia is commonly present in Veterans with post-traumatic stress disorder (PTSD). Treatment of insomnia with a specialized type of psychotherapy has been shown to be more effective than treatment with medications. Unfortunately, few psychologists are trained to provide this treatment, limiting Veterans' access to care, especially those Veterans in remote and rural areas. This project will evaluate the ability to deliver this psychotherapy to groups of Veterans by video teleconferencing. Groups of Veterans with PTSD and chronic insomnia will receive the psychotherapy treatment either by meeting in-person with the psychologist or by the psychologist delivering the treatment by video teleconferencing. Finding that video teleconferencing is a cost effective way to deliver this treatment could add an important new component to the care of Veterans with PTSD that provides an alternative to medications.
Eligibility Criteria
Inclusion Criteria
Veterans will have to meet the following inclusion criteria in order to be enrolled in this RCT:
- Men and women at least 18 years of age.
- Meet current DSM-IV-TR criteria for PTSD as determined by the Clinician Administered PTSD Scale (CAPS)
- Insomnia Severity Index score > 14, the commonly used threshold for clinical insomnia, with self-reported duration of insomnia >6 months.
- Ability to read and speak English (assessment instruments and therapy will be available only in English)
Exclusion Criteria
Veterans will be excluded from participation if they meet any of the following exclusion criteria:
- Unable or unwilling to provide informed consent.
- Unwilling to participate in supervised group sessions at the community based outpatient clinic
- No telephone access or inability to return for follow-up testing.
- Individuals with an untreated sleep disorder [e.g., obstructive sleep apnea (apnea-hypopnea index 15 events/hr), periodic limb movement disorder (10 leg movements/hr of sleep with arousals), central sleep apnea ( 50% of apneas are central), Cheyne-Stokes respiration, obesity hypoventilation syndrome, and narcolepsy].
- A clinically unstable medical condition as defined by a new diagnosis or change in medical management in the previous 2 months.
- Evidence of substance dependence during the preceding twelve months. Evidence of "at risk" drinking behavior over the past month. Namely for men: more than 4 drinks on a given night, drinking on more than 3 nights a week, or more than 14 total drinks in a week; for women: more than 3 drinks in a given night, drinking on more than 3 nights a week, or more than 7 total drinks in a week.
- Individuals with bipolar disorder, delirium, dementia, amnestic disorder, schizophrenia and other psychotic disorders as determined by the SCID questionnaire. A concurrent anxiety disorder or depressive disorder diagnosis will be allowed.
- Individuals with prominent current suicidal or homicidal ideation. This will be assessed by the clinical psychologist administering the SCID and CAPS. In cases of prominent current suicidal or homicidal ideation appropriate safety measures will be taken. Following stabilization, Veterans who continue to be interested in participating in the study may be re-assessed.
- Unable to perform tests due to inability to communicate verbally, inability to read and write; less than a 5th grade reading level; visual, hearing or cognitive impairment (e.g., previous head injury).
Data sourced from ClinicalTrials.gov (NCT01686438). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.