- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06164782
A Survey on Psychosomatic Health Status of Chinese Population
December 15, 2023 updated by: Yonggui Yuan
A Survey on Psychosomatic Health Status of Chinese Population
Study Overview
Status
Not yet recruiting
Detailed Description
This is a nationwide cross-sectional study to investigate psychosomatic symptoms among genral population in China.
This study will also focus on the relationship between psychosomatic symptoms and functions and wellbeing.
Study Type
Observational
Enrollment (Estimated)
300000
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
- Name: Yonggui Yuan, Prof.
- Phone Number: +86-13913939082
- Email: yygylh2000@sina.com
Study Contact Backup
- Name: Lei Li, MD.
- Phone Number: +86-13815434184
- Email: lilei.nj@live.cn
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
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
General population in China
Description
Inclusion Criteria:
- Age 18 years old and above;
- Able to complete the scale independently;
- Subjects read informed consent through online questionnaires and agreed to cooperate with relevant assessments.
Exclusion Criteria:
- Individuals with severe physical disease;
- Individuals with cognitive impairment;
- Individuals who cannot finish the online survay independently.
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
Cohorts and Interventions
Group / Cohort |
|---|
|
General Pupulation of China
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychosomatic health status
Time Frame: Baseline
|
symptoms severity measured by the symptoms checklist of this study
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Yonggui Yuan, Prof., Zhongda Hospital
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)
December 17, 2023
Primary Completion (Estimated)
January 31, 2024
Study Completion (Estimated)
January 31, 2024
Study Registration Dates
First Submitted
December 1, 2023
First Submitted That Met QC Criteria
December 1, 2023
First Posted (Actual)
December 11, 2023
Study Record Updates
Last Update Posted (Actual)
December 22, 2023
Last Update Submitted That Met QC Criteria
December 15, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- CN_Psychosomatic_20231201
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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