- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06912256
The Effects of Individualised Short-term Sleep Restriction on Tactical Performance
March 28, 2025 updated by: José Afonso Coelho Neves
Influence Of Individualized Two Weeks Mild Sleep Restriction On Tactical Performance During Small-Sided Games In National Male Under-19 Football Players: A Randomized Trial
The goal was to evaluate the influence that chronic sleep restriction may have on football players tactical performance during small-sided games.
By using a relative sleep restriction (i.e., by reducing the normal sleep duration by 15%) instead of an absolute sleep restriction (e.g., 3-4 hours), different sleep schedules were applied, according to the players individual sleep profile.
It was hypothesized that the player's performance would be impaired, particularly their tactical behaviors when performing a 4x4 small-sided game format.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
An impairment on cognitive and physical performance is commonly suggested in literature.
However, there is a lack of information regarding sport-specific parameters.
Thus, the present study aimed to examine whether chronic sleep restriction during 9 consecutive days impairs the tactical performance of football players during small-sided games (SSGs).
A total of sixteen national level male football players wore wrist actigraphy units during night sleep throughout the study.
Players were randomized into two groups: intervention (IG), and control (CG).
The first four days corresponded to a familiarization period, where players were informed about the study procedures and started using wrist actigraphy.
Throughout the next seven consecutive days, the characterization phase of sleep players profile (i.e., baseline) was collected and analyzed.
Then, players entered the intervention phase, where the IG slept 15% less than routine.
During this 9-days period, players performed a 4x4 SSGs in two moments (moment 1 and moment 2) with a week interval.
The SSGs were recorded using a video camera and subsequently analyzed using the Game Performance Assessment Instrument.
Study Type
Interventional
Enrollment (Actual)
16
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Porto, Portugal, 4200-450
- Faculty of Sport, University of Porto
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Soccer players classified as Tier 3, corresponding to the National Level in accordance to McKay et al. (2022), as they represented the under-19 team playing in the Portuguese National Championship 1st Division.
Exclusion Criteria:
- 1) players with previously identified sleep disorders;
- 2) players with injuries that prevented them from playing SSGs.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Sleep restriction
During the intervention period (i.e., 9 consecutive days), the intervention group started the sleep protocol, sleeping only the quantity of hours defined for their individual chronic partial sleep restriction (15% of usual daily sleep hours).
The amount and quality of sleep obtained were daily monitored through actigraphy devices, and all the players filled in a sleep diary when they woke up.
During this period, players performed the SSGs in two different moments (moment 1 and moment 2), interspersed by 4 days.
|
During the intervention period (i.e., 9 consecutive days), the intervention group started the sleep protocol, sleeping only the quantity of hours defined for their individual chronic partial sleep restriction (15% of the usual sleep time).
The amount and quality of sleep obtained were daily monitored through actigraphy devices, and all the players filled in a sleep diary when they woke up.
During this period, players performed the SSGs in two different moments (moment 1 and moment 2), interspersed by 4 days.
|
|
No Intervention: Controls
Same intervention (i.e., soccer training and tests) as the other arm, but with no sleep restriction.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Game Performance Assessment Instrument (GPAI)
Time Frame: Applied once in week 1 and once again in week 2
|
According to study purposes, tactical performance was defined as the main variables.
Tactical analysis was performed using the Game Performance Assessment Instrument (GPAI), a tool designed to evaluate the individual tactical behavior (Memmert & Harvey, 2008; Oslin, Mitchell, & Griffin, 1998).
It consists of seven components, two of which are evaluated when the player has the ball and the remaining five when the player does not have the ball possession.
For example, decisions made about what to do with the ball during the game, and motor skill execution were classified as appropriate/efficient or inappropriate/inefficient. The main index proposed by Oslin et al. (1998) was calculated: Game Performance (GP).
Based on actions deemed appropriate or inappropriate, the final score can range from 0 to 100%, with higher values denoting better outcomes.
|
Applied once in week 1 and once again in week 2
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sleep efficiency
Time Frame: Collected daily during the two weeks of the intervention
|
The objective sleep data was collected using three axial accelerometers (ActiGraph LLC wGT3X-BT, Pensacola, USA) placed on the non-dominant wrist.
To analyze the wrist actigraphy data, the ActiLife LLC Pro software (v6.13.3, Pensacola, USA) was used with a sampling frequency of 50Hz and an epoch of activity counts of 60s.
Sleep efficiency (SE, percentage of time in bed that was spent asleep; CV=7%) was determined using the Sadeh's algorithm.
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Collected daily during the two weeks of the intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2023
Primary Completion (Actual)
May 31, 2023
Study Completion (Actual)
December 31, 2023
Study Registration Dates
First Submitted
March 23, 2025
First Submitted That Met QC Criteria
March 28, 2025
First Posted (Actual)
April 4, 2025
Study Record Updates
Last Update Posted (Actual)
April 4, 2025
Last Update Submitted That Met QC Criteria
March 28, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- CEFADE 9 2023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Sensitive data belonging to a club, so we only had permission to report the statistical treatment, but not sharing the IPD.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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