Implementing and Sustaining a Transdiagnostic Sleep and Circadian Treatment
Study Details
Study Description
Brief Summary
The goal is to collect pilot data on an adapted version of the Transdiagnostic Sleep and Circadian intervention (TranS-C), referred to as 'Fitted TranS-C'.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
Mental illness is often severe, chronic and difficult to treat. The sleep disturbance commonly experienced by individuals with a severe mental illness reduces capacity to function and contributes to key symptoms. This study seeks to collect pilot data on an adapted version of the Transdiagnostic Sleep and Circadian intervention (TranS-C). The adapted version will be referred to as 'Fitted TranS-C' as it is designed to improve the fit to delivery within community mental health centers. 'Fitted' treatments are needed because the context for implementation (community setting) typically differs from the original testing context (university setting) causing a lack of 'fit' between the setting and evidence based treatments.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Experimental: Fitted TranS-C Fitted TranS-C involves 4 x 20-30 minute sessions. It involves selected cross-cutting, core and optional modules from Standard TranS-C. |
Behavioral: Fitted Transdiagnostic Sleep and Circadian intervention
Fitted TranS-C is an adapted version is designed to improve the fit with community needs and resources.
Other Names:
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Outcome Measures
Primary Outcome Measures
- The acceptability of the intervention to providers will be assessed by the 'Acceptability of Intervention Measure' (AIM) [4 weeks (i.e. post-treatment assessment)]
The AIM is a measure of the extent to which the intervention is acceptable to providers. The AIM is comprised of 4 questions rated on a 1 'completely disagree' to 5 'completely agree' scale. The responses to all four qus will be reported along with the summed total score.
- PROMIS--Sleep Disturbance (PROMIS = Patient-Reported Outcomes Information System) [Pre-treatment and 4 weeks later (i.e. post-treatment assessment)]
Assesses sleep disturbance experienced by patients
- CEQ (Treatment Evaluation Questionnaire) [4 weeks (i.e. post-treatment assessment)]
Assesses patients' expectations of the treatment.
Secondary Outcome Measures
- Process evaluation/qualitative interview [4 weeks (i.e. post-treatment assessment)]
Assessing the clients' and therapists' opinions of the treatment
- MINI [Baseline only]
Index of psychiatric disorders
Other Outcome Measures
- Referral form [Baseline only]
Assesses participant suitability for the study
Eligibility Criteria
Criteria
Inclusion Criteria:
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Can understand treatment in English
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Is not currently at risk for suicide or homicide
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Has not worked the night shift more than 2 nights per week in the past 3 months
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Is not pregnant or nursing
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Has a guaranteed bed to sleep in for the next month, which is not a shelter.
Exclusion Criteria:
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At risk for suicide or homicide
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Has worked the night shift more than 2 nights per week in the past 3 months
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Is pregnant or nursing
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Does not have a guaranteed bed to sleep in for the next month
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | UC Berkeley | Berkeley | California | United States | 94702 |
Sponsors and Collaborators
- University of California, Berkeley
Investigators
- Principal Investigator: Allison G Harvey, PhD, University of California, Berkeley
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Adapted_MH105513