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Clinical Trials in Sweden / NCT07158138
Starting soon Not applicable

A Digitally Distributed Yoga Intervention in Prostate Cancer Rehabilitation : Protocol for a Randomized Controlled Trial

NCT07158138 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2026-01-10
Last updated
2025-09-05

Condition(s) studied

Prostate Cancer Patients

Investigational drug(s) / intervention(s)

Digital yoga intervention

Digital yoga intervention: Digital yoga intervention

Study summary

Prostate cancer and its treatment can affect psychological, physical, and social quality of life. The most common side effects of the disease and treatment are bowel and urinary problems, sexual issues, and reduced quality of life. These issues can be alleviated with proper treatment and rehabilitation. Stress has been shown to be a significant factor in reduced quality of life.

The overall aim of the research project is to evaluate and compare the effect of an internet-based yoga intervention for individuals diagnosed with prostate cancer with a control group receiving standard care regarding stress, urinary incontinence, blood pressure, and quality of life. Additional objectives include describing cost-effectiveness and the experience of participating in an internet-based yoga intervention at home.

Scientific Questions Does internet-based yoga have any effect on stress, urinary incontinence, blood pressure, and quality of life compared to standard care? Is internet-based yoga a cost-effective intervention from the perspective of healthcare and society compared to standard care? How feasible is internet-based yoga, and how do participants perceive it? Does blood pressure change due to digital yoga, and does the effect persist after one year? Do participants in the intervention group continue practicing yoga after the intervention ends?

Eligibility

Sex
MALE
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: are men diagnosed with prostate cancer without signs of metastatic disease, treated with curative intent. They should be Swedish-speaking and literate. Participants can be included within two months of diagnosis \- Exclusion Criteria: * are individuals under active surveillance or with advanced disease.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Health Care Center Örebro Region Örebro County

More Region Örebro County trials in Sweden

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07158138 on ClinicalTrials.gov ↗ ← All trials in Sweden