NCT07457476

Brief Summary

This will be a longitudinal study that aims to assess the effects of a sleep education and hygiene intervention on the sleep of young soccer players. The primary outcome of interest is the difference-in-differences in objectively measured sleep duration from baseline to post-intervention between the intervention and control groups.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

February 19, 2026

Completed
6 days until next milestone

Study Start

First participant enrolled

February 25, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

March 9, 2026

Completed
27 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 5, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 10, 2026

Completed
Last Updated

March 11, 2026

Status Verified

March 1, 2026

Enrollment Period

1 month

First QC Date

February 19, 2026

Last Update Submit

March 9, 2026

Conditions

Keywords

sleep educationrecoverysportsadolescent

Outcome Measures

Primary Outcomes (2)

  • Sleep duration

    night sleep duration measured with objectively through wrist worn actigraphy devices

    6 weeks

  • Sleep efficiency

    Sleep efficiency measured through wrist worn actigraphy devices. Sleep efficiency is one of the main sleep variables given through actigraphy sleep monitoring and one of the key proxies for sleep quality monitoring.

    6 weeks

Secondary Outcomes (4)

  • Perceived fatigue

    6 weeks

  • Sleep/wake timings

    6 weeks

  • Athlete Sleep Screening Questionnaire.

    At day one and in week 6

  • Sleep Hygiene Index

    At day one and in week 6

Study Arms (2)

Control

NO INTERVENTION

Subjects won't receive sleep education workshops and sleep data

Sleep Education

EXPERIMENTAL

Sbjects will receive sleep education and hygiene sessions, will receive their sleep data and will have objectives

Behavioral: Sleep enhancement intervention

Interventions

Subjects will receive sleep education, sleep hygiene strategies, will have access to their sleep data and will have specific sleep objectives

Also known as: Sleep education, Sleep hygiene
Sleep Education

Eligibility Criteria

Age16 Years - 19 Years
Sexmale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Are actively playing soccer in the under-17 or under-19 of the soccer academy participating in the study.
  • Are between 16 and 19 years old.
  • Are available (i.e., no planned time off) during the monitoring period of the study.

You may not qualify if:

  • Recent history of injury.
  • In injury recovery process (i.e., return to play).
  • Taking any medication that may impact sleep.
  • Has travelled through multiple time zones in the past 3 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

João Barreira, Master

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Doctoral Fellow in the Sport Science Department of the University of Maia

Study Record Dates

First Submitted

February 19, 2026

First Posted

March 9, 2026

Study Start

February 25, 2026

Primary Completion

April 5, 2026

Study Completion

May 10, 2026

Last Updated

March 11, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Data will be anonymized with each participant received a unique identifier code that only the responsible researcher will have access to. IPD data regarding the main study outcomes (sleep, perceptual measures, and sleep questionnaires) will be shared only with the core research team, if necessary, to discuss statistical analysis procedures.