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A digital support program to improve sexual health after pelvic cancer treatment

A digital psychosocial intervention for sexual health after pelvic cancer: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN16919328
Enrollment
240
Registered
2026-05-26
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sexual health problems and reduced sexual wellbeing following treatment for pelvic cancers (prostate, gynaecological, colorectal, and urinary bladder cancer). Urological and Genital Diseases

Interventions

Participants will be randomly assigned to either the intervention or control group with a 1:1 ratio. Stratified randomization will be used
the number of stratification variables will be kept to different cancer types included (colorectal, prostate, gynecological and bladder cancer). A blocked randomization list with four participants per

Sponsors

Linnaeus University
Lead Sponsor
Länssjukhuset i Kalmar
Collaborator
Region Östergötland
Collaborator
Region Jönköpings län
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1. Treated for one of the following pelvic cancer diagnoses: colorectal, prostate, gynaecological or urinary bladder cancer with either surgery, radiation therapy and chemotherapy or a combination of these treatments. 2. Verbally and verified affected sexual health or function with the questionnaire PROMIS Scale v2.0 – Sexual Function Screener. 3. Possess adequate eHealth literacy assessed with the questionnaire eHEALS at baseline. 4. Possess adequate knowledge of the Swedish language. This will be assessed by adequately filling out the screening questionnaires and responses in a brief assessment interview at inclusion. 5. Verbally reported ambition and time to actively work with the rehabilitation intervention for improvements in sexual health. This will be assessed after a brief walkthrough of the intervention regarding the general premise and approximate time needed to complete (around 60 minutes per module/week).

Exclusion criteria

Exclusion criteria: 1. In, or is planned for, active treatment for cancer with chemotherapy, radiation or surgery is planned. 2. Active cancer treatment start during the trial period is a reason for exclusion.

Countries

Sweden

Contacts

Public ContactSamuel Ask
samuel.ask@lnu.se+46 0480446174

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jun 11, 2026