- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05914181
The Relationship Between Self-disclosure, Perceived Social Support and Reproductive Concerns
June 13, 2023 updated by: The First Affiliated Hospital of Soochow University
How Self-disclosure Influences Reproductive Concerns Among Young Male Cancer Patients? The Mediating Role of Perceived Social Support
Participants were recruited from oncology units in two hospitals in Shanxi, China using a convenience sampling.Data were collected using a self-report questionnaire consisting of demographic and disease-related characteristics, and instruments measuring self-disclosure, social support and reproductive concerns.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
200
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: Xingyu Chen, Master
- Phone Number: 18862323110
- Email: 18404998524@163.com
Study Locations
-
-
Shanxi
-
Taiyuan, Shanxi, China, 030200
- Recruiting
- Shanxi Bethune Hospital
-
Contact:
- Xingyu Chen, Master
- Phone Number: 18862323110
- Email: 18404998524@163.com
-
-
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
No
Sampling Method
Non-Probability Sample
Study Population
Participants were recruited from oncology units in two hospitals in Shanxi, China using a convenience sampling.
The eligible participants were invited to complete the questionnaire after they agree to participate.
Description
Inclusion criteria : ① male; ② Age 18-40 years old; ③ Diagnosed with cancer for 1 year or more; ④ Know the disease; ⑤ Clear mind, able to understand and cooperate with the investigation; ⑥ Sign informed consent to participate in the study voluntarily.
Exclusion criteria: ① There were serious primary diseases of liver, kidney, hematopoietic, and serious organ failure; ② He has a history of mental illness, personality disorder, cognitive impairment, and organic brain disease.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Participants characteristics
Time Frame: once
|
Demographic and disease related characteristics included age, marital status, fertility status, payment method of medical expenses, primary caregiver, family history, treatment method, fertility intention, etc.
|
once
|
self-disclosure
Time Frame: once
|
Distress Disclosure Index (DDI) was used to evaluated the level of self-disclosure of young male cancer patients
|
once
|
perceived social support
Time Frame: once
|
the Perceived Social Support Scale (PSSS) was used to evaluate the level of perceived social support of young male cancer patients which includes 3 dimensions which are named by friend support, family support and other support, with a total of 12 items.
|
once
|
reproductive concerns
Time Frame: once
|
the Reproductive concerns after cancer scale-male(RCAC-M) was used to evaluata the level of reproductive concerns in young male cancer survivors.
|
once
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Jun Zhao, The First Affiliated Hospital of Soochow University
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 (Actual)
March 20, 2023
Primary Completion (Estimated)
June 30, 2023
Study Completion (Estimated)
August 1, 2023
Study Registration Dates
First Submitted
June 13, 2023
First Submitted That Met QC Criteria
June 13, 2023
First Posted (Actual)
June 22, 2023
Study Record Updates
Last Update Posted (Actual)
June 22, 2023
Last Update Submitted That Met QC Criteria
June 13, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 20230614
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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