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

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

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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