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Heart rehab gets personal: new program targets Women's sexual Well-Being

NCT ID NCT07426263

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a nurse-led education program designed to help women in cardiac rehab address sexual concerns after a heart event. Sixty-six women will be randomly assigned to either the program or usual care. The goal is to see if the program improves sexual function, mood, and quality of life.

What this could mean

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

Active substance
Therapeutic Education Program on Female Sexuality (PET-SF)
What this could lead to
If it works, this program could become a standard part of cardiac rehab for women, helping them feel better about their sexual health and overall quality of life.
What could go wrong
This is a small, early-stage trial with only 66 participants, so results may not apply to all women. The program is behavioral, so benefits depend on individual engagement.

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 66 people

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

Started

Feb 2026

Expected to finish

May 2027

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

Female participants only

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: Women will be eligible to participate if they meet all of the following criteria: * Female sex. * Age 18 years or older. * Referral to a hospital-based Cardiac Rehabilitation Unit following a cardiovascular event. * Clinical stability and medical clearance to participate in the cardiac rehabilitation program. * Ability to understand the study information and provide written informed consent. Exclusion Criteria: Women will be excluded if any of the following criteria apply: * Severe cognitive impairment or language barriers that preclude understanding of the intervention or study procedures. * Recent participation in structured sexual education or sexual counselling programs. * Inability to attend the sessions assigned within the intervention period. * Attendance at fewer than two sessions of the intervention program. * Occurrence of clinical complications or hospital readmission during the study period that prevent continued participation.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Virgen Macarena University Hospital. Seville (Spain)

    Seville, 41020, Spain

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