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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04198311
Other study ID # 2016896
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 26, 2020
Est. completion date December 31, 2022

Study information

Verified date March 2022
Source University of Missouri-Columbia
Contact Mary E Miller, PhD
Phone 573-882-1813
Email millmary@health.missouri.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Project STAR aims to examine the feasibility, acceptability, and initial efficacy of a CBT-I supplement to outpatient alcohol and substance use treatment.


Description:

Among those who receive treatment for alcohol use disorder (AUD), one in three relapses to problematic drinking within one year of treatment. Thus, additional treatment strategies are needed. Notably, up to 74% of individuals seeking treatment for AUD report co-occurring symptoms of insomnia, while 85% of those seeking SUD treatment report insomnia symptoms. Given the negative impact of insomnia on attention and emotion regulation, insomnia symptoms may decrease patients' abilities to attend to treatment for substance use and manage negative emotions that lead to craving and relapse. This project aims to examine the feasibility, acceptability, and initial efficacy of a CBT-I supplement to substance use treatment. Forty adults who meet diagnostic criteria for AUD or SUD and Insomnia Disorder will receive Cognitive Behavioral Therapy for Insomnia (CBT-I). In order to generate hypotheses regarding the efficacy of CBT-I for individuals who are and are not engaged in substance use treatment, we aim to recruit 20 participants who are engaged in substance use treatment through the community at baseline and 20 participants who are not. Outcomes will be assessed at the end of the active intervention period (6 weeks) and at 6 weeks post-intervention


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
CBT-I
CBT-I will be delivered individually, in five weekly sessions. Intervention components include sleep hygiene, sleep restriction, stimulus control, relaxation, cognitive therapy.

Locations

Country Name City State
United States University of Missouri-Columbia Columbia Missouri

Sponsors (1)

Lead Sponsor Collaborator
University of Missouri-Columbia

Country where clinical trial is conducted

United States, 

Outcome

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)
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