Insomnia Clinical Trial
— STAROfficial title:
The Impact of CBT for Insomnia on Substance Use Treatment Outcomes
Project STAR aims to examine the feasibility, acceptability, and initial efficacy of a CBT-I supplement to outpatient alcohol and substance use treatment.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | December 31, 2022 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Participation in alcohol or substance use treatment in the Columbia, MO area - DSM-5 criteria for moderate to severe Alcohol Use Disorder of Substance Use Disorder - DSM-5 episodic criterion (duration at least 1 month) for Insomnia Disorder Exclusion Criteria: - unable to provide informed consent - cognitive impairment - continuous sobriety for 2+ months at baseline - untreated sleep disorder requiring more than behavioral treatment for insomnia - severe psychiatric disorder that requires immediate clinical attention - initiation of a sleep medication in the past six (6) weeks |
Country | Name | City | State |
---|---|---|---|
United States | University of Missouri-Columbia | Columbia | Missouri |
Lead Sponsor | Collaborator |
---|---|
University of Missouri-Columbia |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Treatment-related Learning | Assessed using the Project STAR alcohol quiz | Change from baseline to post-treatment (week 6) | |
Other | Executive Functioning - Delayed Discounting | Assessed delayed discounting using the Monetary Choice Questionnaire (Kirby, Petry, & Bickel, 1999). Participants are instructed to choose between hypothetically receiving one amount of money today or a larger amount of money in the future. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Other | Executive Functioning - Working Memory | Assessed using the Adaptive N-Back task (Jaeggi et al., 2010).Participants are instructed to indicate if the image they see is the same shape that was presented earlier. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Other | Executive Functioning - Attention | Assessed using the Psycho-motor Vigilance Task (Thomann et al., 2014). Participants are instructed to react to a visual stimulus by quickly pressing a key. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Primary | Recruitment | The number of participants who complete baseline. | Assessed at Post-Treatment (week 6) | |
Primary | Retention | The number of participants who complete all treatment sessions | Assessed at Post-Treatment (week 6) | |
Primary | Treatment Satisfaction | The satisfaction rating participants give the treatment.Assessed using the Client Satisfaction Questionnaire; The Client Satisfaction Questionnaire is an 8-item measure of satisfaction with treatment that has been validated in substance use treatment settings. Items are scores from 1 to 4, with higher scores indicating greater satisfaction with treatment. | Assessed at Post-Treatment (week 6) | |
Secondary | Abstinence | The percentage of days during the past 6 weeks that the participant is abstinent from their drug of choice (alcohol or other substance). Assessed using the Timeline Followback (TLFB); TLFB allows participants to trace their alcohol and drug use back 42 days. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Heavy-Drinking Days | The percentage of days during the past 6 weeks that the participant engages in heavy drinking (>4/5 drinks/day for women/men). Assessed using the Timeline Followback (TLFB) for alcohol; TLFB allows participants to trace their alcohol use back 42 days. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Substance Use Days | The percentage of days during the past 6 weeks that the participant engages in drug/substance use. Assessed using the Timeline Followback (TLFB) ; TLFB allows participants to trace their drug/substance use back 42 days. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Alcohol Problems | Assessed using the Short Inventory of Problems (SIP); SIP measures adverse consequences of substance use. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Alcohol or Other Drugs as Sleep Aids | Assessed using the daily sleep diary; Sleep Diaries are quotidian questionnaires that measure self-reported sleep quality, sleep time, and daily habits concerning substance use. Diaries will be used to determine if participants used alcohol or other substances specifically to go to sleep | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Insomnia severity | Assessed using the Insomnia Severity Index (ISI); ISI will be used as a 7-item measure of insomnia severity in the past two weeks. Items assess difficulty falling or staying asleep, satisfaction with current sleep pattern, interference with daily functioning, the extent to which others notice their sleep problems, and worry/distress related to sleep problems. Response options range from 0 (not at all worried) to 4 (very much worried), with possible total scores ranging from 0 to 28. Participants scoring 10 or higher will be classified as screening positive for insomnia (Morin et al., 2011).114 Notably, self-report is the recommended method of assessment for symptoms of insomnia in adults (Schutte-Rodin et al., 2008). | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Total Wake Time | The amount of time the participant is awake after they try to go to sleep. Measured using Daily Diaries and actigraphy. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Sleep quality | Assessed using the daily sleep diary; Sleep Diaries are quotidian questionnaires that measure self-reported sleep quality, sleep time, and daily habits concerning substance use. Diaries will be used to determine if participants used alcohol or other substances specifically to go to sleep. | Change from baseline to post-treatment (week 6) to follow-up (week 12) | |
Secondary | Dysfunctional beliefs | Assessed using the Dysfunctional Beliefs and Attitudes about Sleep questionnaire (DBAS;Morin, 1994). The DBAS is designed to measure sleep and insomnia-related cognitions. | Change from baseline to post-treatment (week 6) to follow-up (week 12) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04512768 -
Treating Comorbid Insomnia in Transdiagnostic Internet-Delivered Cognitive Behaviour Therapy
|
N/A | |
Recruiting |
NCT05963542 -
Efficacy of Online Acceptance and Commitment Therapy and Sound Therapy for Patients With Tinnitus and Insomnia
|
N/A | |
Completed |
NCT06339853 -
Study of Efficacy of Digital Cognitive Behavioral Therapy With Wearable Device for Insomnia
|
N/A | |
Recruiting |
NCT04069247 -
Effectiveness of eCBT-I on Improving Mental Health in Chinese Youths With Insomnia
|
N/A | |
Completed |
NCT04493593 -
Internet-delivered CBT-I (Space for Sleep): Pilot and Feasibility
|
N/A | |
Recruiting |
NCT06278077 -
Neurexan - a Clinical Trial in Short-Term Insomnia Patients
|
Phase 2 | |
Recruiting |
NCT05956886 -
Sleep Chatbot Intervention for Emerging Black/African American Adults
|
N/A | |
Completed |
NCT04661306 -
The Better Sleep for Supporters With Insomnia Study
|
N/A | |
Recruiting |
NCT06207279 -
Preliminary Study on the Development and Reliability and Validity of Attention Rating Scale
|
||
Recruiting |
NCT06006299 -
Investigating the Use of taVNS to Treat Insomnia in Individuals With Breast Cancer (taVNS-insomnia-BC)
|
N/A | |
Completed |
NCT03683381 -
App-based Intervention for Treating Insomnia Among Patients With Epilepsy
|
N/A | |
Completed |
NCT04564807 -
Testing an Online Insomnia Intervention
|
N/A | |
Completed |
NCT03673397 -
The Acute Effect of Aerobic Exercise on Sleep in Patients With Depression
|
N/A | |
Completed |
NCT04035200 -
Safety, Tolerability and Efficacy Study of V117957 in Subjects With Insomnia Associated With Alcohol Cessation
|
Phase 2 | |
Active, not recruiting |
NCT05027438 -
Reducing Use of Sleep Medications Assisted by a Digital Insomnia Intervention
|
N/A | |
Recruiting |
NCT06053840 -
An Open-label Trial to Evaluate the Safety and Efficacy of Chloral Hydrate in Patients With Severe Insomnia
|
Phase 4 | |
Not yet recruiting |
NCT06348082 -
Project Women's Insomnia Sleep Health Equity Study (WISHES)
|
N/A | |
Not yet recruiting |
NCT06363799 -
Osteopathic Protocol for Insomnia in College Students
|
N/A | |
Not yet recruiting |
NCT06025968 -
Digital Cognitive-behavioral Therapy for Insomnia for Patients With Multiple Sclerosis
|
N/A | |
Not yet recruiting |
NCT05991492 -
Improving Sleep With a Digital Cognitive Behavioral Therapy for Insomnia Application
|
N/A |