Advancing Adolescent Bedtime by MI and Text Reminders
1 other identifier
interventional
212
1 country
1
Brief Summary
Chronic sleep deprivation among adolescents is a prevalent health problem across the world and is associated with a series of short and long term consequences. However, effective interventions targeting on this vulnerable adolescent population is very limited. Majority of the previous sleep education programme are conducted in a school context which personal factors and individualized problems were not addressed. In addition, failure to address "knowledge-action gap" may also explain why individual fail to enact health behaviors even holding positive motivation. In regard to this, investigators proposed an active and person-oriented protocol with the aid of advanced technology in order to improve adolescent sleep health.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2018
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 21, 2018
CompletedFirst Posted
Study publicly available on registry
August 3, 2018
CompletedStudy Start
First participant enrolled
September 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
October 31, 2021
CompletedNovember 30, 2021
November 1, 2021
3.2 years
July 21, 2018
November 28, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change of Sleep duration by sleep diary
Daily sleep diary for consecutive seven days. Sleep parameter estimated by daily sleep diary: total sleep time (TST) in hours
Baseline, 1 week, 3 month and 6 month after treatment
Change of Sleep duration by actigraphy
Sleep parameter estimated by actigraphy: total sleep time (TST) in hours
Baseline, 1 week, 3 month and 6 month after treatment
Secondary Outcomes (10)
Change of Sleep knowledge
Baseline, 1 week, 3 month and 6 month after treatment
Change of Daytime Sleepiness
Baseline, 1 week, 3 month and 6 month after treatment
Change of Quality of Life
Baseline, 1 week, 3 month and 6 month after treatment
Change of Sleep Hygiene
Baseline, 1 week, 3 month and 6 month after treatment
Change of Anxiety and depressive symptoms
Baseline, 1 week, 3 month and 6 month after treatment
- +5 more secondary outcomes
Study Arms (2)
Group MI
EXPERIMENTALThe structure and content of the active intervention programme will be developed and adopted on the basis of previous research on sleep educational programme and motivational interviewing techniques. The whole treatment package consists of 4 sessions of group therapy (n=6-8) followed by 3 week daily text reminders.
Control group
NO INTERVENTIONControl group will no receive any intervention
Interventions
Eligibility Criteria
You may qualify if:
- Chinese aged 12-18 years old
- Written informed consent of participation into the study is given by adolescents and his/her parents;
- Being able to comply with the study protocol;
- Having weekday sleep duration less than 7 hours for past 1 month as reported by questionnaire and average of \<7hr weekday sleep as reported by sleep diary as an indication of chronic sleep deprivation status.
- Possess a mobile phone
You may not qualify 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 clinical 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 such as insomnia, delayed sleep phase and narcolepsy.
- have enrolled in any intervention programme that may affect their sleep patterns in the past three months or are planning to join intervention programme in the next three month
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Chinese University of Hong Konglead
- The University of Hong Kongcollaborator
Study Sites (1)
Department of Psychiatry
Shatin, Hong Kong
Related Publications (1)
Chan NY, Chen SJ, Ngan CL, Li SX, Zhang J, Lam SP, Chan JWY, Yu MWM, Chan KCC, Li AM, Wing YK. Advancing adolescent bedtime by motivational interviewing and text message: a randomized controlled trial. J Child Psychol Psychiatry. 2025 Jul;66(7):1005-1017. doi: 10.1111/jcpp.14115. Epub 2025 Jan 20.
PMID: 39834005DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ngan Yin Chan, Mphi
Chinese University of Hong Kong
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The assessor will be blinded to the condition of the subjects
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Associate
Study Record Dates
First Submitted
July 21, 2018
First Posted
August 3, 2018
Study Start
September 1, 2018
Primary Completion
October 31, 2021
Study Completion
October 31, 2021
Last Updated
November 30, 2021
Record last verified: 2021-11
Data Sharing
- IPD Sharing
- Will not share