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Not yet recruitingNCT07873203Updated Oct 14, 2026

Delayed Morning Training, Sleep, and Change-of-Direction Performance in Badminton Athletes

An interventional study of Usual Morning Training Schedule and Delayed Morning Training Schedule in Sleep Duration and Athletic Performance, sponsored by Capital University of Physical Education and Sports, China. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-14.

Sponsored by Capital University of Physical Education and Sports, China · Not applicable, Interventional, and Other

Updated Oct 14, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
38
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

This randomized controlled trial will investigate whether delaying the start of morning training from 7:00 AM to 9:00 AM improves nocturnal sleep and change-of-direction performance in elite badminton athletes. A total of 38 athletes with an established morning-training routine will be randomly assigned in a 1:1 ratio to either a usual morning-training group starting at 7:00 AM or a delayed morning-training group starting at 9:00 AM. Both groups will follow the same training content, duration, intensity, coaching arrangements, and recovery procedures for three weeks.

Nocturnal sleep will be objectively monitored using wrist-worn activity monitors, with total sleep time as the primary outcome. Change-of-direction performance will be assessed using the modified 505 test. Additional outcomes will include sleep opportunity, sleep efficiency, sleep onset latency, nighttime awakenings, bedtime and wake time, nap duration, 24-hour total sleep, training load, and training adherence.

The study aims to determine whether a later morning-training schedule can provide athletes with greater sleep opportunity without compromising training quality or physical performance.

Read the detailed description

This study is a two-arm, parallel-group, individually randomized controlled trial designed to evaluate the effects of delaying morning training on sleep and change-of-direction performance in elite badminton athletes.

Thirty-eight athletes with a stable morning-training routine will be enrolled and randomly allocated in a 1:1 ratio to a usual morning-training group or a delayed morning-training group. Randomization will be stratified by sex and recruitment batch using concealed variable block sizes. The study will be conducted in two recruitment batches, with the second batch starting approximately four weeks after the first. Outcome assessors, sleep-data scorers, and statistical analysts will be blinded to the actual group allocation.

Before randomization, participants will complete health and injury screening, sleep-disorder risk screening, questionnaires, and a baseline monitoring period. Wrist-worn activity monitors will be used to objectively assess sleep. Participants will also complete sleep diaries documenting bedtime, sleep timing, nighttime awakenings, wake time, naps, device removal, caffeine and alcohol intake, medications or supplements, illness, pain, additional training, and other events that may affect sleep.

During the 3-week intervention period, both groups will complete five morning-training sessions per week, for a total of 15 sessions. The usual morning-training group will begin training at 7:00 AM, whereas the delayed morning-training group will begin at 9:00 AM. Each morning session will last approximately 90 minutes. Apart from the assigned training start time, the two groups will follow the same daily training plan, including training content, duration, sets, rest intervals, venue, equipment, coaching arrangements, afternoon training, dietary principles, and recovery procedures.

The primary outcome will be objectively measured nocturnal total sleep time during the intervention period. The key secondary outcome will be change-of-direction performance assessed using the modified 505 test. The modified 505 test will be conducted before and after the intervention under standardized conditions. Each athlete will complete three valid trials, and the fastest valid completion time will be used as the main performance measure.

Additional sleep-related outcomes will include sleep opportunity, sleep efficiency, sleep onset latency, nighttime awakenings, bedtime, wake time, nap duration, and 24-hour total sleep. Training load, training adherence, session rating of perceived exertion, protocol deviations, injuries, and adverse events will also be recorded.

The primary analysis will follow the intention-to-treat principle. The primary sleep outcome will be compared between groups using analysis of covariance adjusted for baseline sleep duration, sex, and recruitment batch. The post-intervention modified 505 outcome will also be analyzed using analysis of covariance adjusted for baseline performance, sex, and recruitment batch. Repeated nightly sleep measurements will additionally be analyzed using linear mixed-effects models. Effect estimates will be reported with 95% confidence intervals.

02

Conditions studied

  • Sleep Duration
  • Athletic Performance

Keywords

  • Badminton
  • Elite Athletes
  • Morning Training
  • Training Start Time
  • Sleep Duration
  • Nocturnal Sleep
  • Change-of-Direction Performance
  • Modified 505 Test
  • Training Load
  • Sleep Monitoring
03

In context

Lead sponsor

Capital University of Physical Education and Sports, China is the lead sponsor of 9 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Elite badminton athletes receiving systematic professional badminton training and able to competently perform the modified 505 change-of-direction test.
  • A stable morning-training schedule during the previous 4 weeks.
  • Ability to maintain the same training phase, training location, and accommodation conditions throughout the study period.
  • Ability to complete baseline monitoring, the 3-week intervention, and pre- and post-intervention assessments.
  • Ability to understand the study procedures and willingness to provide written .

Exclusion criteria

Exclusion Criteria:

  • Injury or musculoskeletal condition that prevents safe completion of maximal-effort change-of-direction testing.
  • Unstable cardiovascular, neurological, or other health conditions.
  • Deemed unsuitable for maximal-effort training or testing by sports medicine personnel.
  • Planned participation in a major competition, off-site training camp, or trans-time-zone travel during the study period.
  • A previously diagnosed sleep disorder.
  • Inability to comply with activity-monitor wear, sleep-diary completion, or assigned training-time requirements.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
38 participants (estimated)

Study arms

  • Active comparator
    Usual Morning Training Group

    Participants assigned to the usual morning-training group will continue their regular morning-training schedule, beginning training at 7:00 AM. They will complete five morning-training sessions per week for three consecutive weeks, for a total of 15 sessions. Each session will last approximately 90 minutes. Training content, duration, sets, rest intervals, venue, equipment, coaching arrangements, afternoon training, dietary principles, and recovery procedures will be standardized and matched to those of the delayed morning-training group.

    Behavioral: Usual Morning Training Schedule

  • Experimental
    Delayed Morning Training Group

    Participants assigned to the delayed morning-training group will begin morning training at 9:00 AM, representing a 120-minute delay compared with the usual 7:00 AM schedule. They will complete five morning-training sessions per week for three consecutive weeks, for a total of 15 sessions. Each session will last approximately 90 minutes. No mandatory roll call, early class, group activity, or other required task will be scheduled before the 9:00 AM training session. Training content, duration, sets, rest intervals, venue, equipment, coaching arrangements, afternoon training, dietary principles, and recovery procedures will otherwise be matched to those of the usual morning-training group.

    Behavioral: Delayed Morning Training Schedule

Interventions

  • BehavioralUsual Morning Training Schedule

    Participants assigned to the usual morning-training group will begin each scheduled morning training session at 7:00 AM. The intervention will last for 3 consecutive weeks, with five morning-training sessions per week and 15 sessions in total. Each session will last approximately 90 minutes and will include standardized warm-up, badminton-specific technical training, footwork and change-of-direction exercises, multi-shuttle or tactical training, and cool-down. Training content, duration, workload, rest intervals, coaching arrangements, venue, diet, and recovery procedures will be matched to those of the delayed morning-training group.

  • BehavioralDelayed Morning Training Schedule

    Participants assigned to the delayed morning-training group will begin each scheduled morning training session at 9:00 AM, representing a 120-minute delay from the usual 7:00 AM schedule. The intervention will last for 3 consecutive weeks, with five morning-training sessions per week and 15 sessions in total. Each session will last approximately 90 minutes and will follow the same standardized training content and workload as the usual morning-training group. No mandatory roll call, early class, group activity, or other required task will be scheduled before the 9:00 AM training session.

06

What researchers measure

Primary outcomes

  1. Average Nocturnal Total Sleep Time During the Intervention Period

    Nocturnal total sleep time will be objectively measured using a wrist-worn activity monitor. Total sleep time is defined as the total number of minutes classified as sleep within the main nocturnal sleep period, excluding periods classified as wakefulness. The primary outcome will be calculated for each participant as the mean nocturnal total sleep time across valid target nights during the 3-week intervention period. Higher values indicate longer nocturnal sleep duration.

    Time frame: Throughout the 3-week intervention period, from Day 1 through Day 21

Secondary outcomes

  1. Modified 505 Change-of-Direction Test Completion Time

    Change-of-direction performance will be assessed using the modified 505 test under standardized conditions. Each participant will complete three valid trials, and the fastest valid completion time will be used as the outcome value. Completion time will be measured in seconds using electronic timing gates. Lower values indicate better change-of-direction performance.

    Time frame: Day 22, after the 3-week intervention

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — Individual participant data are not planned for public sharing. To protect participant confidentiality in this relatively small cohort of elite athletes, access to individual-level data will be restricted to the study team in accordance with the approved protocol and data-management procedures. Study results will be reported in aggregate form.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Jan 2027, 2 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 6, 2026
First posted
Oct 14, 2026
StartEst.
Nov 1, 2026
Primary completionEst.
Jan 30, 2027
CompletionEst.
Jan 30, 2027
Last update
Oct 14, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 14, 2026
Show all 1 update
  1. Oct 14, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07873203
Lead sponsor
Capital University of Physical Education and Sports, China
Responsible party
Tongwu Yu (Principal Investigator, Capital University of Physical Education and Sports, China) — Principal investigator
First posted
Oct 14, 2026
Start date
Nov 1, 2026 (estimated)
Primary completion
Jan 30, 2027 (estimated)
Completion
Jan 30, 2027 (estimated)
Last update
Oct 14, 2026

Study contacts

Tongwu Yu, PhD
Contact
18101351378@163.com
+86 18101351378

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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