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Low-Intensity Scheduled Morning Exercise for Adolescents with a Late Chronotype: A Novel Treatment to Improve Sleep Health?

Low-Intensity Scheduled Morning Exercise for Adolescents with a Late Chronotype: A Novel Treatment to Improve Sleep Health?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00025322
Enrollment
24
Registered
2021-05-12
Start date
2016-06-05
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Late chronotype

Interventions

Group 1: 45-minutes low-intensity morning exercise in dim-light (<10 lux) approximately 10-15 minutes after awakening. Low-intensity exercise (walking on a treadmill) is individually defined at 30% to

Sponsors

University of Basel, Department of Sport, Exercise, and Health
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
15 Years to 18 Years

Inclusion criteria

Inclusion criteria: Male Aged 15-18 years absence of sleep and other psychological disorders sedentary: < 60 min physical activity per week Late chronotype

Exclusion criteria

Exclusion criteria: Physical conditions that need medical advice before being physically active (e.g., resting heart rate > 90 BPM), intake of psychopharmaceuticals, as some antidepressants impact the biotransformation of melatonin. Female adolescents will not be considered for recruitment, as modification in circadian rhythms across the menstrual cycle require an assessment during the luteal phase. Being bound to the school holiday period, this would impose significant organizational challenges. A further exclusion criteria is a physically active individual (>60min moderate-to-vigorous physical activity per week) and having a early or regular chronotype

Design outcomes

Primary

MeasureTime frame
Dim light melatonin onset (DLMO) is measured via salivary DLMO samples taken half-hourly in dim light (<10 lux) using salivettes (Sarstedt, Newton, NC, USA) starting 4 hrs before and finishing 2 hrs after adolescent`s bedtime (Crowley et al., 2016). Participants are seated for at least 5 min before and during each saliva sample, to minimize the masking effects of physical movement on endogenous melatonin production. Food and water are consumed only after saliva collection to reduce contamination or dilution of the sample. Participants are instructed to place the swab in their mouth and accumulate saliva for 2 min. After collection, samples will be stored frozen at -20°C. This procedure will be replicated during follow-up assessments. For analysis, samples will be thawed and centrifuged for 10 min at 2500 rpm, the swabs removed from the casing, and the supernatant retained. A sensitive (4.3 pM) direct radioimmunoassay (RIA) using reagents from Buhlmann Laboratories AG (Allschwil, Switzerland) (Voultsios et al., 1997) will be used to measure melatonin in the saliva.

Secondary

MeasureTime frame
1. Evening sleepiness will be assessed subjectively via the Karolinskia Sleepiness Scale (KSS; Åkerstedt & Gillberg, 1990) in the 3 hrs before bedtime. 2. Objective evening vigilance will be measured immediately after each KSS rating. The computerized Go/NoGo task (E-Prime v1.2, Psychology Software Tools, Inc., Pittsburgh, PA, USA, 2006) measures sustained attention in relation to inhibitory functions and consists of two visual stimuli presented in random order. 3. Mood/daytime functioning will be assessed via the Depression, Anxiety, and Stress Scale (DASS-21) to detect secondary outcomes of morning exercise and/or circadian phase shift on mood.

Countries

Australia

Contacts

Public ContactChristin Lang

University of Basel, Department of Sport, Exercise, and Health

christin.lang@unibas.ch+41791092274

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026