NCT03614572

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
212

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2018

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
13 days until next milestone

First Posted

Study publicly available on registry

August 3, 2018

Completed
29 days until next milestone

Study Start

First participant enrolled

September 1, 2018

Completed
3.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2021

Completed
Last Updated

November 30, 2021

Status Verified

November 1, 2021

Enrollment Period

3.2 years

First QC Date

July 21, 2018

Last Update Submit

November 28, 2021

Conditions

Keywords

Sleep deprivationMotivational InterviewingText reminders

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

EXPERIMENTAL

The 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.

Behavioral: Group MI

Control group

NO INTERVENTION

Control group will no receive any intervention

Interventions

Group MIBEHAVIORAL

refer to the arm description

Also known as: Motivational interviewing
Group MI

Eligibility Criteria

Age12 Years - 18 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

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

Study Sites (1)

Department of Psychiatry

Shatin, Hong Kong

Location

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.

MeSH Terms

Conditions

Sleep Deprivation

Interventions

Motivational Interviewing

Condition Hierarchy (Ancestors)

DyssomniasSleep Wake DisordersNervous System DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMental Disorders

Intervention Hierarchy (Ancestors)

Directive CounselingCounselingMental Health ServicesBehavioral Disciplines and ActivitiesHealth ServicesHealth Care Facilities Workforce and Services

Study Officials

  • Ngan Yin Chan, Mphi

    Chinese University of Hong Kong

    PRINCIPAL INVESTIGATOR

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

Locations