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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ANZCTR
Last refreshed on: 13 January 2020
Main ID:  ACTRN12615000061538
Date of registration: 23/01/2015
Prospective Registration: Yes
Primary sponsor: Kate Bartel
Public title: The use of constructive worry and mindfulness body scan for helping adolescent sleep
Scientific title: The use of constructive worry or mindfulness body scan compared to bedtime as normal, for helping adolescents' sleep.
Date of first enrolment: 26/05/2015
Target sample size: 300
Recruitment status: Stopped early
URL:  https://anzctr.org.au/ACTRN12615000061538.aspx
Study type:  Interventional
Study design:  Purpose: Treatment; Allocation: Randomised controlled trial;  
Phase:  Not Applicable
Countries of recruitment
Australia
Contacts
Name: Dr Kate Bartel   
Address:  School of Psychology Flinders University GPO Box 2100 Adelaide SA 5001 Australia
Telephone: +61 8 8201 3435
Email: kate.bartel@flinders.edu.au
Affiliation: 
Name: Dr Kate Bartel   
Address:  School of Psychology Flinders University GPO Box 2100 Adelaide SA 5001 Australia
Telephone: +61 8 8201 3435
Email: kate.bartel@flinders.edu.au
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: Over 14 years of age, attending high school.
Exclusion criteria: Taking medication that interferes with sleep. Currently attending treatment for a sleep disorder or anxiety.

Age minimum: 14 Years
Age maximum: 20 Years
Gender: Both males and females
Health Condition(s) or Problem(s) studied
Sleep;
Sleep
Mental Health - Other mental health disorders
Intervention(s)
Constructive worry: 15 minutes per evening, between the hours of 6-8pm, of documenting worries/concerns, followed by ways to resolve these. Daily for two weeks.
Mindfulness body scan: 15 minutes of practicing a mindfulness body scan at normal bedtime, each day for two weeks.

Both groups will be given instructions immediately after completion of their baseline data, via the computer screen. The researcher will be present at the time, to answer any questions.

Adherence will be monitored by a twice-off self-report questionnaire.
Primary Outcome(s)
Total sleep time, measured by a self-report questionnaire, based on the School Sleep Habits Survey (Wolfson & Carskadon, 1998).[Baseline, one and two weeks post randomisation.]
Sleep onset latency, measured by a self-report questionnaire, based on the School Sleep Habits Survey (Wolfson & Carskadon, 1998).[Baseline, one and two weeks after randomisation. ]
Pre-sleep cognitive and emotional arousal. Measured by the Pre-sleep Arousal Scale and the Adolescent Sleep Hygiene Scale- revised.[Baseline, one and two weeks post randomisation.]
Secondary Outcome(s)
Daytime functioning. Measure by the Chronic Sleep Reduction Questionnaire - short form.[Baseline, one and two weeks post randomisation.]
Secondary ID(s)
Nil known
Source(s) of Monetary Support
Flinders University
Secondary Sponsor(s)
A/Prof Michael Gradisar
Ethics review
Status: Approved
Approval date:
Contact:
Social and Behavioural Research Ethics Committee
Results
Results available:
Date Posted:
Date Completed:
URL:
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