Sleep Clinical Trial
Official title:
Recovery Sleepers: A Pilot Study of a Sleep Health Intervention for College Students in Recovery
Verified date | December 2022 |
Source | Virginia Commonwealth University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this research study is to examine how to improve sleep in college students in recovery from substance use disorder(s). This study is a pilot test of an experimental program called Recovery Sleepers (RS) to explore its feasibility and how well it works to improve sleep, wellbeing, and cravings.
Status | Completed |
Enrollment | 12 |
Est. completion date | October 3, 2022 |
Est. primary completion date | October 3, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - More than 18 years of age - Enrolled (full- or part-time) at a college or university - Have struggled with substance addiction in the past - More than 3 months of self-reported continuous abstinence from alcohol and all illegal drugs - Have an Internet-enabled device with audio capabilities. Exclusion Criteria: - Younger than 18 years of age - Not enrolled at VCU - Have not struggled with substance addiction in the past - Have not had at least 3 months of self-reported continuous abstinence from alcohol and all - illegal drugs - In active treatment for a sleep disorder (seen a health provider specifically regarding sleep within the last 6 months) - Unable to communicate in English both orally and in writing - Do not have an Internet-enabled device with audio capabilities. |
Country | Name | City | State |
---|---|---|---|
United States | Virginia Commonwealth University | Richmond | Virginia |
Lead Sponsor | Collaborator |
---|---|
Virginia Commonwealth University | Society for Health Psychology |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Satisfaction with treatment | Participants will rate their experiences in the study using a scale from 1 (Strongly disagree) to 5 (Strongly agree). Treatment and placebo groups will answer a different number of questions. Scores will be averaged to yield a single score between 1 and 5. | 6 weeks | |
Primary | Study participant retention | Percent of participants who complete all 6 weeks of the study | 6 weeks | |
Primary | Study material completion | Percent of participant who complete all of the study materials over the course of the study | 6 weeks | |
Primary | Study group attendance | Percent of participants who attend all study group meetings | 6 weeks | |
Primary | Recruitment success | Number of participants recruited into the study | Baseline |
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