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New online program STORK seeks to boost new Parents' sex lives

NCT ID NCT07344454

Prevention Sponsor: Dalhousie University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Aug 28, 2026 · Updated 3 times

Summary

This study tests an online program called STORK designed to help couples maintain their sexual well-being during the transition to parenthood. The program includes weekly modules during pregnancy and one after birth, covering common sexual changes and relationship skills. Researchers will enroll 268 couples expecting their first baby to see if the program improves sexual satisfaction, reduces distress, and supports overall relationship health compared to a waitlist group.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
online psychoeducation program
What this could lead to
If it works, this could provide an accessible, evidence-based tool to help new parents maintain their sexual and relationship well-being during a challenging life transition.
What could go wrong
This is a relatively small, early-stage trial with no blinding, and the program is compared to a waitlist control, so results may be influenced by expectations. The program may not work for all couples or in all cultural contexts.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 268 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2026

Expected to finish

Mar 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

puerperal disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Postpartum Pregnancy

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Dalhousie University

    RECRUITING

    Halifax, Nova Scotia, B3H4R2, Canada

  • University of British Columbia

    RECRUITING

    Vancouver, British Columbia, V6T 1Z4, Canada

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