Effectiveness of a Sleep Hygiene Education in Female Para Athletes

February 26, 2026 updated by: Ahmet Sansi, Abant Izzet Baysal University

Effectiveness of a Sleep Hygiene Education in Female Para Athletes: A Mixed-Methods Study Using PSQI, Sleep Behaviour, and Qualitative Experiences

It is imperative to recognise elite female sitting volleyball players as a high-risk group with regard to sleep deprivation. However, there is a paucity of research investigating the efficacy of sleep hygiene education for this demographic.

The objective of this study is to The present study aims to examine the effect of sleep hygiene education on sleep quality and behaviour in elite female sitting volleyball players using mixed methods.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

The method of this study will consist of a mixed design conducted on athletes selected from the Turkish Women's National Sitting Volleyball Team using purposive sampling. The Pittsburgh Sleep Quality Index (PSQI) will be utilised to assess the participants' sleep quality, while the Athlete Sleep Behavior Questionnaire (ASBQ) will be employed to evaluate their sleep behaviours. Data collection will be conducted at two distinct time points: firstly, prior to the implementation of a structured sleep hygiene education programme, and subsequently approximately 30 days thereafter, which will be designated as the post-test phase. In order to provide a more in-depth elucidation of the quantitative findings and to achieve a more contextualised understanding, qualitative data will be collected through two online focus group discussions following the post-test.

Study Type

Interventional

Enrollment (Estimated)

12

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 Contact

Study Contact Backup

Study Locations

    • Province
      • Bolu, Province, Turkey (Türkiye), 14030
        • Bolu abant Izzet Baysal University

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being an elite athlete who is a member of the Turkey Women's National Sitting Volleyball Team.
  • Actively participating in regular training sessions and competitions.
  • Willingness to participate in the planned sleep hygiene education program throughout the study period.
  • Having sufficient cognitive capacity to complete the Pittsburgh Sleep Quality Index (PSQI) and the Athlete Sleep Behavior Questionnaire (ASBQ).
  • Agreeing to participate in focus group interviews.
  • Providing voluntary participation and signing an informed consent form.

Exclusion Criteria:

  • Inability to participate regularly in training sessions during the study period due to acute injury, illness, or surgical intervention.
  • Failure to attend the education program or assessment procedures regularly.
  • Incomplete completion of data collection instruments or non-participation in focus group interviews.

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Turkish women's national sitting volleyball team
The study's sample population will comprise all athletes who will be members of the Turkish national sitting volleyball team in the 2026 season. The selection of participants will be carried out using a purposive sampling method, and data will be collected from all volunteers who will be willing to participate in the study and who will meet the specified criteria. This approach will result in the establishment of a sample group that will reflect the full characteristics of the target population.

The method of this study will consist of a mixed-method design conducted with athletes selected from the Turkish Women's National Sitting Volleyball Team through purposive sampling. The Pittsburgh Sleep Quality Index (PSQI) will be used to assess participants' sleep quality, while the Athlete Sleep Behavior Questionnaire (ASBQ) will be employed to evaluate their sleep behaviours. Data will be collected at two distinct time points: first, prior to the implementation of a structured sleep hygiene education program, and subsequently approximately 30 days later, designated as the post-test phase.

In order to provide a more in-depth explanation of the results obtained from the quantitative data and to achieve a more contextual understanding, qualitative data will be collected through two online focus group discussions conducted following the post-test.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Sleep Behavior Scores as Measured by the Turkish Version of the Athlete (Sleep Behavior Questionnaire (ASBQ).
Time Frame: Baseline (Pre-intervention) and Approximately 30 days after the intervention.

Measurement Tool: The ASBQ is a 17-item five-point Likert-type questionnaire used to assess athletes' sleep habits. This tool identifies abnormal patterns and areas for improvement in an athletic context.

This scale allows athletes to evaluate their own sleep behavior through self-assessment.

Scoring Interpretation: The scale is evaluated based on the total score. A total score of 34 or below indicates "good sleep behavior," while a total score of 40 or above indicates "poor sleep behavior."

Unit of Measure: Total Score on the ASBQ (Range: 17 to 85).

Baseline (Pre-intervention) and Approximately 30 days after the intervention.
Change from Baseline in Global Sleep Quality Score Assessed by the Pittsburgh Sleep Quality Index (PSQI)
Time Frame: Baseline (Pre-intervention) and Approximately 30 days after the intervention.

The PSQI is a self-rated questionnaire that assesses sleep quality and disturbances over a 1-month time interval. It consists of 19 individual items that generate seven distinct component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. Each component score is weighted equally on a scale from 0 to 3. These seven component scores are then summed to yield a single global PSQI score, which has a possible range of 0 to 21. A global score of 5 or less indicates "good sleep quality," while a score greater than 5 indicates "poor sleep quality." Therefore, higher global scores represent worse sleep quality and greater sleep difficulties.

Unit of Measure: Global Score (Range: 0 to 21)

Baseline (Pre-intervention) and Approximately 30 days after the intervention.
Qualitative Assessment of Behavioral Changes and Sleep Hygiene Perceptions via Semi-Structured Focus Group Interviews
Time Frame: Conducted after the 30-day post-test data collection.

To complement the quantitative findings within a mixed-methods design, qualitative data will be collected through online focus group discussions. These sessions will utilize semi-structured interview guides specifically designed to explore participants' underlying sleep habits, their behavioral changes post-intervention, and their overall perceptions of sleep hygiene. The qualitative data (transcripts) will be subjected to thematic analysis to identify recurring patterns, context, and relationships. Unlike quantitative measures, this assessment does not yield a numerical score; instead, it generates descriptive narrative themes that evaluate the real-world effectiveness and subjective experience of the training program.

Unit of Measure: Qualitative Themes and Narrative Feedback (Descriptive/Categorical)

Conducted after the 30-day post-test data collection.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Social Jetlag (SJL) Calculated by Mid-Sleep Time Discrepancy
Time Frame: Baseline (Pre-test) and Approximately 30 days after the intervention (Post-test).

Social Jetlag (SJL) quantifies the misalignment between an individual's biological circadian clock and their social or work schedules. It is determined by calculating the absolute difference between the mid-point of sleep on free days (MSF) and the mid-point of sleep on workdays (MSW). The mid-point of sleep is defined as the exact halfway point between sleep onset and wake time (e.g., if sleep onset is 24:00 and wake time is 08:00, the mid-point is 04:00). The specific calculation formula used is:Social Jetlag is calculated based on the difference between the mid-point of sleep on free days (MSF) and the mid-point of sleep on workdays (MSW). The calculation formula is as follows: SJL = |MSF - MSW|.

Unit of Measure: Time difference (Expressed in Hours and Minutes)

Baseline (Pre-test) and Approximately 30 days after the intervention (Post-test).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Ahmet Sansi, PhD, Bolu Abant Izzet Baysal University Sport Science Faculty

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 (Estimated)

February 27, 2026

Primary Completion (Estimated)

February 27, 2026

Study Completion (Estimated)

March 30, 2026

Study Registration Dates

First Submitted

February 13, 2026

First Submitted That Met QC Criteria

February 26, 2026

First Posted (Actual)

February 27, 2026

Study Record Updates

Last Update Posted (Actual)

February 27, 2026

Last Update Submitted That Met QC Criteria

February 26, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AIBU-ANE-AS-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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