NCT07802093

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

87
On Track

Trial Health Score

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

Enrollment
18

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2025

Shorter than P25 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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 2, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 14, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 14, 2025

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

August 25, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 3, 2026

Completed
Last Updated

September 3, 2026

Status Verified

August 1, 2026

Enrollment Period

1 month

First QC Date

August 25, 2026

Last Update Submit

August 30, 2026

Conditions

Keywords

Recovery strategiesfatiguesportyouth athletes

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

EXPERIMENTAL
Other: Compression LeggingsOther: Compression Calf SleevesOther: Placebo

Sequence 2: Calf Sleeves - Placebo - Leggings

EXPERIMENTAL
Other: Compression LeggingsOther: Compression Calf SleevesOther: Placebo

Sequence 3: Placebo - Leggings - Calf Sleeves

EXPERIMENTAL
Other: Compression LeggingsOther: Compression Calf SleevesOther: Placebo

Interventions

Participants wore fullcompression leggings from approximately two hours before bedtime until waking for seven consecutive nights.

Sequence 1: Leggings - Calf Sleeves - PlaceboSequence 2: Calf Sleeves - Placebo - LeggingsSequence 3: Placebo - Leggings - Calf Sleeves

Participants wore compression calf sleeves from approximately two hours before bedtime until waking for seven consecutive nights.

Sequence 1: Leggings - Calf Sleeves - PlaceboSequence 2: Calf Sleeves - Placebo - LeggingsSequence 3: Placebo - Leggings - Calf Sleeves
PlaceboOTHER

Participants wore visually similar non-compressive placebo garments from approximately two hours before bedtime until waking for seven consecutive nights.

Sequence 1: Leggings - Calf Sleeves - PlaceboSequence 2: Calf Sleeves - Placebo - LeggingsSequence 3: Placebo - Leggings - Calf Sleeves

Eligibility Criteria

AgeUp to 18 Years
Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

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

Location

MeSH Terms

Conditions

Fatigue

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

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
Model Details: All participants first completed a one-week baseline control condition without garments. Participants subsequently completed three one-week garment conditions (compression leggings, compression calf sleeves, and placebo garments) in a randomized crossover order.
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

Locations