Clinical trial Recruiting at 1 site Interventional Ages 18 and up Men only

E-Mergir: a digital program to support mental and sexual health for prostate cancer survivors

Official title: E-Mergir: a Randomized Controlled Trial to Test the Efficacy of a Digital Psychosexual Intervention for the Promotion of Mental and Sexual Health of Prostate Cancer Survivors

Run by Universidade do Porto · NCT07754929 · Data updated 2026-11-12

A digital CBT-based program called E-Mergir is tested in prostate cancer survivors to see if it improves sexual and mental well-being compared with a wait-list control.

More Prostate Cancer trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexMen only
Enrollment106 (estimated)
SponsorUniversidade do Porto
Academic / other
Locations1 site (Porto)
StatusRecruiting
StartedJuly 1, 2026
Main results expectedJanuary 1, 2027
Study endsJuly 1, 2027
Registry record updatedAugust 10, 2026
Trial IDNCT07754929 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adult prostate cancer survivors with smartphone and internet access, no recent other cancers or severe psychiatric conditions, and who are willing to participate in an online program.

Probably not a fit

Patients with severe neurological or psychiatric disorders, ongoing psychotherapy, other active cancer treatments, or sensory impairments limiting online use may not benefit.

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

What this trial studies

This randomized controlled trial tests a digital, CBT- and mindfulness-based psychosexual intervention for men who have survived prostate cancer. The program, delivered online over eight weeks with five modules, includes psychoeducation, sexual rehabilitation, mindfulness, cognitive restructuring, and relapse prevention, guided by a certified clinical psychologist. Participants are randomly assigned to receive the E-Mergir program or be on a wait-list control, with assessments at baseline, post-intervention, and follow-up using validated sexual and mental-health measures. Recruitment occurs through the Urology department at Coimbra University Hospital, and eligibility requires prostate cancer survivorship, 18 years or older, smartphone use, internet access, and no recent other cancers. The study is led by Universidade do Porto and is conducted in Porto, Portugal.

Why it matters

Potential benefit: If successful, participants may experience improved sexual satisfaction, reduced distress, and better overall quality of life.

How similar studies have gone: Digital psychosexual and CBT-based online interventions have shown promise in related populations, supporting the potential for benefit in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Prostate cancer survivors,
* 18 years old or older,
* Ability to give informed consent,
* Regular use of a smartphone and internet access.

Exclusion Criteria:

* Other diagnosed oncological diseases over the past five years,
* Severe neurological impairment or other severe psychological/psychiatric diseases (depression, generalized anxiety disorder, psychosis-related disorders),
* Other uncontrolled/unstable diseases,
* Severe hearing and/or visual impairment,
* Under psychotherapy or treatment for sexual problems,
* Participating concurrently in other clinical trials.

Where it's running

  • Faculdade de Psicologia e de Ciências da Educação da Universidade do Porto
    Porto, Portugal
    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.