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Prevention study for Insomnia
Official title Prevention of Insomnia in At-risk Youth
ClinicalTrials.gov ID: NCT05451524
What this study is testing
- What it's testing
- This study aims to conduct a randomized controlled trial in comparing cognitive behavioral insomnia prevention program with the active control group in youths who are at risk of insomnia. The results of this study will allow us to take this potential efficacious prevention program to scale and reduce the associated burden of insomnia in the future.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 15 to 24. Healthy volunteers may be eligible.
You may be able to join if
- Youth aged between 15-24 years (as defined by WHO);
- Written informed consent of participation into the study is given by youth and his/her parents if under 18 years old; In addition, individual assent...
- Have subclinical insomnia symptoms (at least once a month but less than 3 times/week in the past one month);
- At least one of the biological parents with current or lifetime history of insomnia disorder as defined by DSM-V diagnostic criteria.
You likely can't join if
- A current or past history of neuropsychiatric disorder(s);
- A prominent medical condition or taking medication with potential side effects that may influence sleep quantity and quality;
- Having a diagnosed sleep disorder that may potentially contribute to the disruption of sleep quantity and quality as ascertained by both Structured...
- Having a clinically significant suicidality (presence of suicidal ideation with a plan or an attempt);
- Currently receiving any structured psychotherapy;
- With hearing or speech deficit;
See the full eligibility criteria
- Youth aged between 15-24 years (as defined by WHO);
- Written informed consent of participation into the study is given by youth and his/her parents if under 18 years old; In addition, individual assent will also be obtained for people under age 18 years old;
- Have subclinical insomnia symptoms (at least once a month but less than 3 times/week in the past one month);
- At least one of the biological parents with current or lifetime history of insomnia disorder as defined by DSM-V diagnostic criteria.
- A current or past history of neuropsychiatric disorder(s);
- A prominent medical condition or taking medication with potential side effects that may influence sleep quantity and quality;
- Having a diagnosed sleep disorder that may potentially contribute to the disruption of sleep quantity and quality as ascertained by both Structured Diagnostic Interview for Sleep patterns and Disorders (DISP) such as...
- Having a clinically significant suicidality (presence of suicidal ideation with a plan or an attempt);
- Currently receiving any structured psychotherapy;
- With hearing or speech deficit;
- Trans-meridian flight in the past 3 months and during the study.
The study team makes the final eligibility decision.
Where it's taking place
- Shatin, NT, Hong Kong
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 15 years to 24 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Shatin, NT, Hong Kong. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.