Does Wearing Compression Garments Affect Sleep in Soccer Players
2 other identifiers
interventional
18
1 country
1
Brief Summary
This study investigated the effects of nocturnal compression garments on sleep quantity and quality in young elite male soccer players. Eighteen players participated in a randomized controlled crossover protocol conducted over four consecutive weeks. During the first week, participants completed a control condition without wearing compression garments. During the following three weeks, they completed three experimental conditions in randomized order: full compression leggings, compression calf sleeves, and non-compressive placebo garments. Each condition was performed for seven consecutive nights. Objective sleep parameters were assessed using actigraphy, while subjective sleep quality was evaluated using validated self-report measures. Training load, perceptual factors, pre-sleep nutrition, and nocturnal thermal conditions were monitored and controlled to limit potential confounding factors. The primary objective was to determine whether nocturnal compression garment use affects sleep quantity and quality in young elite soccer players.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 14, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 14, 2025
CompletedFirst Submitted
Initial submission to the registry
August 25, 2026
CompletedFirst Posted
Study publicly available on registry
September 3, 2026
CompletedSeptember 3, 2026
August 1, 2026
1 month
August 25, 2026
August 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Total Sleep Time
Assessed nightly during each 7-night condition
Time in Bed
Assessed nightly during each 7-night condition
Sleep Latency
Assessed nightly during each 7-night condition
Mean Sleep Efficiency Assessed by Wrist Actigraphy
Sleep efficiency was assessed by wrist actigraphy and calculated as the percentage of time in bed spent asleep. Nightly sleep efficiency values were averaged across the seven consecutive nights of each experimental condition. Higher values indicate greater sleep efficiency.
Measured nightly and averaged across the 7 consecutive nights of each condition
Number of Nocturnal Awakenings
Assessed nightly during each 7-night condition
Subjective Sleep Quality Assessed Using the Sleep Item of the Hooper Questionnaire
Subjective sleep quality was assessed using the sleep-quality item of the Hooper Questionnaire (Hooper et al., 1995). Participants rated the quality of the previous night's sleep on a 7-point Likert-type scale ranging from 1 (very, very good) to 7 (very, very bad), with higher scores indicating poorer perceived sleep quality.
Assessed nightly during each 7-night condition
Study Arms (3)
Sequence 1: Leggings - Calf Sleeves - Placebo
EXPERIMENTALSequence 2: Calf Sleeves - Placebo - Leggings
EXPERIMENTALSequence 3: Placebo - Leggings - Calf Sleeves
EXPERIMENTALInterventions
Participants wore fullcompression leggings from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore compression calf sleeves from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore visually similar non-compressive placebo garments from approximately two hours before bedtime until waking for seven consecutive nights.
Eligibility Criteria
You may qualify if:
- Residence at the professional soccer academy throughout the study period.
- Abstinence from tobacco and alcohol throughout the study period.
- No caffeine intake within 12 hours before bedtime.
You may not qualify if:
- Sustaining an injury during the study period.
- Exposure to a training load substantially different from that of the rest of the group.
- Development or presence of a sleep deficit during the study period.
- Failure to consume the standardized evening meal provided at the academy cafeteria.
- Consumption of caffeine, tobacco, or alcohol during the study period.
- Removal of the assigned garment or actigraphy device during the night.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centre technique et sportif de la Gaillette Gervais Martel
Avion, 62210, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Participants were blinded to the compressive or non-compressive nature of the garments. The initial no-garment baseline condition was not blinded.
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
August 25, 2026
First Posted
September 3, 2026
Study Start
November 2, 2025
Primary Completion
December 14, 2025
Study Completion
December 14, 2025
Last Updated
September 3, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share