- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06839417
Effect of Squash Exercise Intervention on Sleep and Mental Health Among Young Adults
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
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Yanwei You, PhD
- Phone Number: +86-17315218175
- Email: yyw22@mails.tsinghua.edu.cn
Study Locations
-
-
-
Beijing, China, 100084
- Tsinghua
-
Contact:
- Yanwei You, PhD
- Phone Number: 17315218175
- Email: yyw22@mails.tsinghua.edu.cn
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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