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Supporting Couples' Perinatal Sexual Well-being: Testing the Introductory Modules of a Novel Prevention Program (STORK)

NCT07036484 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 22

Last updated 2025-07-02

No results posted yet for this study

Summary

Most new parents will experience changes to their sexual relationship during the perinatal period, yet no accessible prevention programs exist to support couples in navigating these changes. The goal of this observational study is to test the feasibility of the introductory modules of an online program (STORK) designed to promote perinatal sexual well-being in a sample of expectant couples. The main question it aims to answer is:

Is STORK a feasible and acceptable resource to support couples' perinatal sexual well-being? Couple participants who complete the first two modules of the STORK program will answer online survey questions and an interview about their experience with the program.

Conditions

  • Pregnancy

Interventions

BEHAVIORAL

Online program

We tested the feasibility of the introductory modules of an online couple-based program (STORK), designed to be grounded in empirically established risk and protective factors associated with couples' perinatal sexual well-being. STORK is a web-based program including psychoeducation and behavioral tasks to be completed by couples

Sponsors & Collaborators

  • University of British Columbia

    collaborator OTHER

  • Dalhousie University

    lead OTHER

Principal Investigators

  • Natalie O Rosen, Ph.D. · Dalhousie University, Canada

  • Samantha J Dawson, Ph.D. · University of British Columbia, Canada

  • Inês M Tavares, Ph.D. · Lusófona University, Portugal

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-11
Primary Completion
2023-12-08
Completion
2023-12-08

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07036484 on ClinicalTrials.gov