Effect of Squash Exercise Intervention on Sleep and Mental Health Among Young Adults

February 16, 2025 updated by: Yanwei You, Tsinghua University

Dear Squash Enthusiast, Hello!

First of all, thank you for participating in this survey! This questionnaire is part of a joint study conducted by the Sports and Brain Science Research Team at Tsinghua University and the Squash program students from Nanjing Sport Institute. The study focuses on promoting squash, understanding the exercise experiences of squash participants, and examining the effects of squash on sleep and mental health. Completing the questionnaire will take approximately 5 minutes.

This research strictly follows the guidelines of the Tsinghua University Ethics Review Committee. All tests are harmless to the body, and there are no right or wrong answers to the questions in the survey. Please respond according to your personal situation. Your personal information will only be used for statistical purposes, and we will ensure that your information is kept strictly confidential.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

100

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 Locations

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • (1) healthy young adults ; (2) without chronic diseases or psychiatric disorders between the ages of 18 and 35; (3) absence of regular exercise for the past half year; (4) right-handedness; (5) Neither color blindness nor color weakness exist.

Exclusion Criteria:

  • the exclusion criteria includes individuals with a history of cardiovascular, metabolic, or neurological disorders (such as hypertension, diabetes, epilepsy, or other significant medical conditions), as well as those with current or past psychiatric disorders, including depression, anxiety, schizophrenia, or other mood or behavioral disorders. Participants who have engaged in regular physical exercise or athletic training within the past six months will also be excluded, as their activity levels may interfere with the results. Left-handed individuals will be excluded, as handedness can affect motor performance and brain activity patterns. Additionally, individuals with any visual impairment affecting color perception, such as color blindness or color weakness, will be excluded. Those currently using medications that affect cognitive function, mood, or physical performance (e.g., antidepressants, anxiolytics, or beta-blockers) will also be excluded, as will individuals with a history of substance abuse or current substance use. Participants with sleep disorders, such as insomnia or sleep apnea, will be excluded to avoid confounding sleep-related outcomes. Lastly, pregnant or breastfeeding individuals, as well as those currently participating in other clinical trials or studies that could interfere with this research, will be excluded from the study.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: control
Experimental: exercise
two group two test
using squash exercise

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
sleep quality
Time Frame: 3 MONTH
PSQI
3 MONTH

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
mental health
Time Frame: 3 MONTH
PHQ9
3 MONTH

Collaborators and Investigators

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

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)

March 1, 2025

Primary Completion (Estimated)

March 1, 2027

Study Completion (Estimated)

March 1, 2027

Study Registration Dates

First Submitted

February 9, 2025

First Submitted That Met QC Criteria

February 16, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 16, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2024THZWYY05

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

This study aims to investigate the effects of squash exercise intervention on sleep and mental health. The research will be conducted in two phases. First, we will conduct a cross-sectional survey to assess the baseline relationship between squash participation and sleep quality, as well as mental well-being. Following this, a randomized controlled trial will be implemented, starting with a one-time intervention to observe immediate effects of squash exercise on sleep and mental health. Subsequently, a 10-week intervention will be conducted, with three sessions per week, each lasting one hour, to explore the long-term impact of regular squash exercise on these outcomes. The goal is to provide insights into how squash as a form of physical activity can influence sleep patterns and mental health.

IPD Sharing Time Frame

From 2025 March to 2027 March

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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