Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

Support for the transition to Parenthood with Online Sex and Relationship Knowledge

Official title: STORK (Supporting the Transition to Parenthood Through Online Sex and Relationship Knowledge) Randomized Controlled Trial

Run by Dalhousie University · NCT07344454 · Data updated 2026-11-12

This program tests STORK, an online resource aimed at helping expecting couples manage sexual well-being during the transition to parenthood.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment268 (estimated)
SponsorDalhousie University
Academic / other
Locations2 sites (Vancouver, British Columbia and 1 other locations)
StatusRecruiting
StartedJanuary 22, 2026
Main results expectedMarch 2029
Study endsMarch 2029
Registry record updatedAugust 27, 2026
Trial IDNCT07344454 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are new or expectant couples in a committed relationship, where one partner is 13–27 weeks pregnant with their first child, fluent in English, and able to access email.

Probably not a fit

Couples experiencing severe relational distress or not completing baseline assessments may not benefit from the program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial investigates an online intervention called the STORK Program designed for couples where one partner is pregnant. It uses a structured online curriculum to address sexual satisfaction, intimacy, and communication during pregnancy through 12 months postpartum. Participants are married or cohabiting couples in a first pregnancy with low-risk status, recruited from Canada, the U.S., Australia, New Zealand, Ireland, and the U.K. The study analyzes whether the program improves sexual well-being and relationship quality compared with standard information, with baseline and follow-up assessments to track changes. The trial aims to inform resources for couples navigating changes in sexuality and intimacy across the transition to parenthood.

Why it matters

Potential benefit: If successful, the program could help couples maintain intimacy and reduce perinatal stress during the transition to parenthood.

How similar studies have gone: Previous related work on online relationship resources has shown mixed results, with this study testing a theory-driven, postpartum-followed approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* married or cohabitating romantic relationship of at least 12 months
* one member of the couple must be currently pregnant (13-27 weeks gestation) with their first baby together (If the couple has a history of miscarriage or stillbirth, previously gave a baby up for adoption, or have other children who do not live with them, they are still eligible to participate.)
* low-risk pregnancy
* live in Canada, the United States, Australia, New Zealand, the Republic of Ireland, or the United Kingdom
* able to read and understand English
* have access to a personal e-mail account

Exclusion Criteria:

* severe relational distress or conflict as determined by baseline measures
* one or both partners of a couple do not complete the baseline survey - this includes cases where one or both partners do not pass at least 3/5 attention checks in the baseline survey
* instructed to avoid sexual activity from a healthcare professional

Where it's running

  • University of British Columbia
    Vancouver, British Columbia, Canada
    Recruiting
  • Dalhousie University
    Halifax, Nova Scotia, Canada
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.