- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05751239
Motives for Desiring Children in Different Sexual-romantic Orientations
March 2, 2023 updated by: University Hospital Inselspital, Berne
Motives for Desiring Children in Different Sexual-romantic Orientations: A Cross-sectional Study
The goal of this cross-sectional study is to compare the motives for the desire to have children in different sexual-romantic orientation. The main question[s] it aims to answer are:
- Do all orientations have the same motives for the desire to have children?
- What are the preferred methods for having a child for the different orientations
Participants will answer an online questionaire .
Researchers will compare the different orientations to see if there are differences.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
837
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bern, Switzerland, 3010
- Department of Obstetrics and Gynecology, lnselspital, Bern University Hospital, University of Bern
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
LGBT+ organisations and groups in Switzerland and social media were contacted for the participants' recruitment.
Description
Inclusion Criteria:
- All participants regardless of sex, gender or age
Exclusion Criteria:
- Incomplete questionnaire
- Under 18 years
- Caring for a child in a social, economic or educational way (self-report)
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 |
|---|---|
|
Bisexual-Biromantic
People that self-identify as bisexual-biromantic
|
All participants answered an online questionaire.
Out of the 837 participants 641 were included
|
|
Heterosexual-heteroromantic
People that self-identify as heterosexual-heteroromantic
|
All participants answered an online questionaire.
Out of the 837 participants 641 were included
|
|
Homosexual-homoromantic
People that self-identify as homosexual-homoromantic
|
All participants answered an online questionaire.
Out of the 837 participants 641 were included
|
|
Pansexual-panromantic
People that self-identify as pansexual-panromantic
|
All participants answered an online questionaire.
Out of the 837 participants 641 were included
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Possible difference in the motive to have a child between different orientations.
Time Frame: At baseline in July/August 2018
|
The questionnaire, that was answered at baseline, included statements that people rated.
There were 5 statement each for each motive and 10 additional statements
|
At baseline in July/August 2018
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Preferred way to have a child of the different orientations
Time Frame: At baseline in July/August 2018
|
People with positive wish for child could choose from different possibilities their preferred method (assessed via questionnaire).
|
At baseline in July/August 2018
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Petra Stute, Dr. med., Department of Obstetrics and Gynecology, lnselspital, Bern University Hospital, University of Bern
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)
July 3, 2018
Primary Completion (Actual)
August 30, 2018
Study Completion (Actual)
August 30, 2018
Study Registration Dates
First Submitted
February 20, 2023
First Submitted That Met QC Criteria
February 20, 2023
First Posted (Actual)
March 2, 2023
Study Record Updates
Last Update Posted (Estimate)
March 6, 2023
Last Update Submitted That Met QC Criteria
March 2, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- BASEC 201800535
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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