Current Awareness, Perspective and Knowledge on Social Egg Freezing

November 11, 2024 updated by: Chung Pui Wah Jacqueline, Chinese University of Hong Kong
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.

Study Overview

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

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

Study Contact Backup

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

Sampling Method

Probability Sample

Study Population

All patients aged from 18-60 years old, who have undergone or will seek fertility preservation services in PWH and the general public will be invited to participate.

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

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
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

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

Investigators

  • Principal Investigator: Pui Wah Jacqueline Chung, Chinese University of Hong Kong

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)

September 1, 2024

Primary Completion (Estimated)

August 31, 2029

Study Completion (Estimated)

September 1, 2030

Study Registration Dates

First Submitted

August 22, 2024

First Submitted That Met QC Criteria

August 30, 2024

First Posted (Actual)

September 3, 2024

Study Record Updates

Last Update Posted (Estimated)

November 12, 2024

Last Update Submitted That Met QC Criteria

November 11, 2024

Last Verified

November 1, 2024

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)?

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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