The First-Night Effect and Sex Differences in Strength and Muscular Endurance Performance
The First-Night Effect: Sex Differences in the Impact of Unfamiliar Sleeping Environment on Strength and Muscular Endurance Performance in Resistance-trained Participants
1 other identifier
interventional
32
1 country
1
Brief Summary
Introduction: The first-night effect, characterized by disturbed sleep in an unfamiliar environment, may impair next-day physical performance. However, whether this response differs between men and women remains unclear. This study investigated sex differences in the effects of sleeping in an unfamiliar environment on strength and muscular endurance in resistance-trained individuals. Methods: Thirty-two resistance-trained participants (16 women, 16 men; 23 ± 4 years) completed a randomized, counterbalanced crossover study involving two conditions: sleeping for 8 h at home or in the laboratory. The following morning, participants performed bench press and back squat strength tests across 25-90%1RM, followed by muscular endurance tests to failure at 65%1RM.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2024
Typical duration 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
February 7, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 3, 2026
CompletedFirst Submitted
Initial submission to the registry
August 5, 2026
CompletedFirst Posted
Study publicly available on registry
August 11, 2026
CompletedAugust 11, 2026
August 1, 2026
1.9 years
August 5, 2026
August 5, 2026
Conditions
Outcome Measures
Primary Outcomes (5)
Mean velocity at different %1RM
Mean velocity at different %1RM (25%, 50%, 75%, 90%)
Through study completion, an average of 3 weeks
Number of repetitions performed during 1 set at 65%1RM until task failure
In bench press and back squat exercises
Through study completion, an average of 3 weeks
Bar velocity deplacement performed in 1 set at 65%1RM until task failure
In bench press and back squat exercises
Through study completion, an average of 3 weeks
Handgrip and isometric mid-thigh pull tests
N generated
Through study completion, an average of 3 week
Vertical Jump test (CMJ)
cm of Height and W/kg generate during a CMJ
Through study completion, an average of 3 week
Secondary Outcomes (1)
Mood state (tension, depression, anger, vigor, fatigue and confusion)
Through study completion, an average of 3 weeks
Study Arms (2)
8h Sleep at home
PLACEBO COMPARATORParticipants sleep 8h at home
8h Sleep at the Laboratory
EXPERIMENTALParticipants sleep 8h at the laboratory
Interventions
Participants sleep 8h at the laboratory
Eligibility Criteria
You may qualify if:
- Age between 18 and 35 years.• Body Mass Index (BMI) \< 25 kg/m².
- Resistance-trained individuals (more than 2 years of structured training).
- Healthy men and women without neurological, cardiometabolic, immunological, or physical conditions that prevent them from exercising.
- Participants must be able to perform the tests described in the following section.
You may not qualify if:
- History of neuromuscular diseases, heart disease, or conditions that may affect liver or muscle metabolism.
- Use of drugs, stimulants, or sports supplements that could interfere with the dietary supplement used in the study.
- Sedentary habits (less than 150 minutes/week of moderate exercise).• Having undergone prolonged periods of physical inactivity in the 6 months prior to the study.
- Engaging in strenuous exercise within 48 hours prior to the tests.• Failure to replicate the same food intake on both experimental days.
- Consumption of caffeine or any other stimulant the day before the tests.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Facultad de Medicina y Ciencias de la Salud. Universidad de Alcalá
Alcalá de Henares, Madrid, 28805, Spain
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Masking Details
- Investigador and Statistician were blinded
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
August 5, 2026
First Posted
August 11, 2026
Study Start
February 7, 2024
Primary Completion
December 20, 2025
Study Completion
May 3, 2026
Last Updated
August 11, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will share