- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06581666
Current Awareness, Perspective and Knowledge on Social Egg Freezing
Study Overview
Status
Conditions
Detailed Description
Hong Kong's fertility preservation service is underutilized and limited, with low awareness among clinicians and young adults. Traditional Chinese culture may lead to social stigma, preventing discussion of fertility issues. A survey aims to explore awareness, knowledge, and acceptance of oocyte cryopreservation, enabling resource allocation for a culturally acceptable public education program and a dedicated referral system to improve oocyte cryopreservation services.
The questionnaire will be in paper form and as an online survey. Potential participants will be provided with the study aim and respondent rights. Once verbal informed consent is obtained, participants will be asked to fill in the self-administered questionnaire. For the online survey, implied consent from the participants will be adopted when they complete the questionnaire on the webpage and return it to us.
In order to reach the 2 target groups, convenient sampling will be used. Questionnaires will be distributed to the patients who have undergone or will seek fertility preservation services in PWH. For the general public, they will be recruited online via an invitation link.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: PUI WAH JACQUELINE CHUNG
- Phone Number: +852 35051537
- Email: jacquelinechung@cuhk.edu.hk
Study Contact Backup
- Name: Elaine Yee Lee NG
- Phone Number: +852 35052745
- Email: elaineng@cuhk.edu.hk
Study Locations
-
-
-
Hong Kong, Hong Kong
- Recruiting
- Pui Wah Jacqueline Chung
-
Contact:
- PUI WAH JACQUELINE CHUNG
- Phone Number: +852 35051537
- Email: jacquelinechung@cuhk.edu.hk
-
Contact:
- Elaine Yee Lee NG
- Phone Number: +852 35052745
- Email: elaineng@cuhk.edu.hk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- People with aged from 18-60 years old
Exclusion Criteria:
- Patients unable to provide consent/assent (i.e. significant psychiatric problems/cognitive delay)
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
All patients who have undergone or will seek fertility preservation services
All patients who have undergone or will seek fertility preservation services, but they will be asked to complete the same set of questionnaires.
|
No special intervention, all participants will be asked to complete same set of questionnaire.
|
|
General public
The general public will also be asked to complete the sane set of questionnaires.
|
No special intervention, all participants will be asked to complete same set of questionnaire.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Awareness, perspective and knowledge
Time Frame: through study completion, an average of 1 year
|
To evaluate the difference in the level of awareness, perspective and knowledge towards social egg freezing between patients who have undergone or will seek fertility preservation services and the general public.
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Awareness
Time Frame: through study completion, an average of 1 year
|
To evaluate the awareness of oocyte cryopreservation among the general public and patients
|
through study completion, an average of 1 year
|
|
Factors that may affect the uptake rate
Time Frame: through study completion, an average of 1 year
|
To determine any factors that may affect the uptake rate of oocyte cryopreservation
|
through study completion, an average of 1 year
|
|
Utilization rate
Time Frame: through study completion, an average of 1 year
|
To assess the utilization rate of social egg freezing
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Pui Wah Jacqueline Chung, Chinese University of Hong Kong
Study record dates
Study Major Dates
Study Start (Actual)
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2024.346
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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