NCT06223776

Brief Summary

The study aims to see how acute sleep restriction will affect women resistance trainers. Above all, the investigators will be interested in observing the relationship between shorter sleep and athletic performance, as well as other important aspects, such as their level of motivation to exercise, how much pain participants felt during exercise and how demanding they found exercise. The investigators assume that differences in subjective measures (such as pain levels, motivation and mood) will be most apparent.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2023

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 15, 2023

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

November 10, 2023

Completed
3 months until next milestone

First Posted

Study publicly available on registry

January 25, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2024

Completed
Last Updated

April 11, 2024

Status Verified

April 1, 2024

Enrollment Period

1.2 years

First QC Date

November 10, 2023

Last Update Submit

April 10, 2024

Conditions

Keywords

acute sleep restrictionearly sleep restriction

Outcome Measures

Primary Outcomes (4)

  • Maximal strength bench press test

    The next day after a) sleep restriction b) normal sleep

    1 day after night with or without intervention

  • Muscle endurance test in bench press

    muscle endurance test in the bench press exercise at 50% 1RM

    1 day after night with or without intervention

  • Explosive bench press exercise

    three sets of three repetitions of explosive bench press exercise at 50% of the load representing one-repetition maximum (1RM)

    1 day after night with or without intervention

  • Countermovement jump

    Vertical jump test performed by having an athlete quickly squat to a self-selected depth and then jump as high as possible.

    1 day after night with or without intervention

Secondary Outcomes (6)

  • Mood (POMS)

    1 day after night with or without intervention

  • Pain (Pain scale)

    1 day after night with or without intervention

  • Motivation

    1 day after night with or without intervention

  • Rating perceived exertion (RPE)

    1 day after night with or without intervention

  • Stress and recovery (SRSS)

    1 day after night with or without intervention

  • +1 more secondary outcomes

Other Outcomes (8)

  • Objective Sleep - Total sleep time

    1 day after night with or without intervention

  • Objective Sleep - Sleep efficiency

    1 day after night with or without intervention.

  • Objective Sleep - WASO (Wake After Sleep Onset)

    1 day after night with or without intervention.

  • +5 more other outcomes

Study Arms (2)

Normal sleep

NO INTERVENTION

The night before the experimental session, where participants will follow their habitual sleep-wake routines.

Sleep restriction

EXPERIMENTAL

The night before the experimental session (with sleep restrictions (SR)), where participants will experience acute sleep restriction the night before the test session (i.e., 3 h of early sleep restriction versus normal sleep).

Procedure: Sleep restriction

Interventions

Participants will experience a night of acute sleep restriction. During this night, they will sleep 3 hours less than usual.

Sleep restriction

Eligibility Criteria

Age18 Years - 30 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • a minimum of 3 years of training experience;
  • practicing physical activity for the last 6 months at least 3 times per week for 2h
  • current medical qualification for competitive sport

You may not qualify if:

  • diseases that can have a bad influence on the menstrual cycle (e.g. polycystic ovarian syndrome, endometriosis);
  • using hormonal contraception;
  • regularity of the menstrual cycle.
  • diagnosed cardiovascular, metabolic, gastrointestinal, or neurological diseases;
  • movement, neuromuscular or musculoskeletal disorders;
  • taking medications and supplements that may affect fitness test results;
  • taking supplements that may affect biochemical test results
  • sleep disorders
  • PSQI \>5

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University School of Physical Education in Cracow

Krakow, 31-571, Poland

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Purpose
DIAGNOSTIC
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 10, 2023

First Posted

January 25, 2024

Study Start

May 15, 2023

Primary Completion

August 1, 2024

Study Completion

August 1, 2024

Last Updated

April 11, 2024

Record last verified: 2024-04

Locations