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Cognitive FunctionsNCT07857720

Cognitive Functions in Women's National Sitting Volleyball Players

A study testing Multidimensional Sleep Hygiene Optimization Protocol in people with Cognitive Functions, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study investigates the effects of a multidimensional, 13-component sleep hygiene optimization intervention on cognitive performance (executive functions, cognitive flexibility, and psychomotor speed) and objective sleep parameters in elite female sitting volleyball athletes. Read more about this study

Who is it for?
Ages 18 years and older, women onlyHealthy volunteers can take part
Conditions the study is for
Cognitive Functions
What is being tested?
Multidimensional Sleep Hygiene Optimization Protocol
Could I receive a placebo?
No, everyone receives an active treatment
How many people
8 participants
Where
1 siteTurkey (Türkiye)
Study dates
10 Apr 2026to 25 Apr 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • ≥ 18 years of age
  • Active national sitting volleyball team member
  • ≥ 1 year of national team experience
  • ≥ 20 hours of weekly training

Who cannot join

  • Non-compliance with the team camp program
  • Major neurological diagnosis

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Bolu Abant Izzet Baysal University Spor Science Faculty

    Bolu, 14000

Other trials in Turkey (Türkiye)

About this study

Official title: Effects of a Sleep Environment Optimization Intervention on Cognitive Functions in Women's National Sitting Volleyball Players

This study investigates the effects of a multidimensional, 13-component sleep hygiene optimization intervention on cognitive performance (executive functions, cognitive flexibility, and psychomotor speed) and objective sleep parameters in elite female sitting volleyball athletes. The study aims to optimize the on-court decision-making mechanisms of Paralympic athletes by improving sleep quality through structured environmental and behavioral factors.

Read the detailed description

Quick decision-making, attention, and executive control are of critical importance in elite sports performance, and these neurocognitive functions are highly dependent on high-quality sleep. While the literature generally focuses on athletes without physical disabilities, evidence regarding sleep optimization for Paralympic athletes-who often experience specific physiological challenges such as chronic pain or spasticity-is limited. This research was conducted during the competition preparation period with athletes from the Turkish Women's National Sitting Volleyball Team (n=8). The study utilized a single-group pre-test/post-test experimental design, applying a specific sleep hygiene intervention consisting of 13 components. The effectiveness of the intervention was systematically analyzed using objective cognitive tests evaluating processing speed, attention, and executive control (Symbol Digit Modalities Test and Stroop Test), alongside objective sleep parameters obtained via wearable technology (Xiaomi Mi Band 7).

Being tested
Multidimensional Sleep Hygiene Optimization Protocol
Keywords
Cognitive Function, Para-Athete

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Multidimensional Sleep Hygiene Optimization ProtocolBehavioural

    This protocol includes the following 13 rules, with participants' compliance monitored daily via a checklist over 5 working days: (1) Ceasing the use of electronic devices 1 hour before sleep, (2) Avoiding vigorous exercise before sleep, (3) Optimizing room temperature between 18-22°C, (4) Turning off all light-emitting devices, (5) Using a sleep mask, (6) Not using the bedroom for work purposes during the day, (7) Avoiding unhealthy snacks before sleep, (8) Cutting off caffeine intake at least 3 hours before sleep, (9) Engaging in adequate daily exercise, (10) Practicing pre-sleep stress management techniques, (11) Ensuring a quiet sleep environment, (12) Establishing a personalized pre-sleep routine (e.g., brushing teeth), and (13) Not taking daytime naps.

Study groups in NCT07857720
Study groupRoleWhat they receive
Sleep enviroment intervention /Experimental Group (Turkish Women's National Sitting Volleyball Team)Experimental* Intervention Type: Behavioral (Behavioral and Environmental Modification) * Intervention Name: 13-Component Multidimensional Sleep Hygiene Optimization Protocol This protocol includes the following 13 rules, with participants' compliance monitored daily via a checklist over 5 working days: (1) Ceasing the use of electronic devices 1 hour before sleep, (2) Avoiding vigorous exercise before sleep, (3) Optimizing room temperature between 18-22°C, (4) Turning off all light-emitting devices, (5) Using a sleep mask, (6) Not using the bedroom for work purposes during the day, (7) Avoiding unhealthy snacks before sleep, (8) Cutting off caffeine intake at least 3 hours before sleep, (9) Engaging in adequate daily exercise, (10) Practicing pre-sleep stress management techniques, (11) Ensuring a quiet sleep environment, (12) Establishing a personalized pre-sleep routine (e.g., brushing teeth), and (13) Not taking daytime naps.
Receives: Behavioral: Multidimensional Sleep Hygiene Optimization Protocol

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Objective Cognitive Performance Analysis using the Symbol Digit Modalities Test (SDMT) and Stroop Test (TBAG Form)

    Visual scanning and psychomotor speed (total substitutions, correct substitutions, number of errors) were recorded using the SDMT. Executive functions, cognitive flexibility, and response inhibition (task completion times in seconds, number of spontaneous corrections, and number of errors) were recorded using the Stroop Test. A decrease in completion times and an increase in accuracy rates indicate improved cognitive performance.

    Measured: Baseline (Day 0), Mid-intervention (Day 3), and immediately after the 5-day intervention (Day 8)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Oct 2026
  2. Study start10 Apr 2026
  3. Primary completion10 Apr 2026
  4. Study completion25 Apr 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Model description
The study sample will consist of all athletes who will be part of the Turkish women's sitting volleyball national team members for the 2026 season. The selection of participants will be conducted using a sampling method, and data will be collected from all volunteers who are willing to participate and meet the specified criteria. This approach will ensure the creation of a sample group that reflects all the characteristics of the target population. Once the volunteer participants have been identified, the researchers aim to optimize the sleep environment in collaboration with the coaches of them.
Masking
None (open label)
Enrolment
8 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07857720
Sponsor's protocol ID
AIBU-ANE-AS-02
Status last verified
Sep 2026
First submitted
22 Sep 2026
Last updated
5 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Multidimensional Sleep Hygiene Optimization Protocol in people with Cognitive Functions, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Objective Cognitive Performance Analysis using the Symbol Digit Modalities Test (SDMT) and Stroop Test (TBAG Form) (time frame: Baseline (Day 0), Mid-intervention (Day 3), and immediately after the 5-day intervention (Day 8)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Oct 2026.

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