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Prostate Cancer PatientsDigiyoga-PNCT07158138

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

A study testing Digital yoga intervention in people with Prostate Cancer Patients, run by Region Örebro County at 1 site in Sweden.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Any age, men only
Conditions the study is for
Prostate Cancer Patients
What is being tested?
Digital yoga intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
220 participants
Where
1 siteSweden
Study dates
10 Jan 2026to 10 Jan 2030
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Men only
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • are individuals under active surveillance or with advanced disease.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Emma Ohlsson-Nevo, A. professor contact

+460704366788

emma.ohlsson-nevo@regionorebrolan.se

Sweden1 site
  • University Health Care Center

    Örebro, Region Örebro County, 70185

    0761065843, emma.ohlsson-nevo@regionorebrolan.se

Other trials in Sweden

About this study

Official title: A Digitally Distributed Yoga Intervention in Prostate Cancer Rehabilitation (DigiYoga-P): Protocol for a Randomized Controlled Trial

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?

Read the detailed description

There are no studies evaluating the effect of digital yoga in individuals diagnosed with prostate cancer.

The study is a randomized controlled multicenter study, where participants are randomized to an internet-based yoga intervention or a control group.

Study Participants Inclusion criteria are men diagnosed with prostate cancer without signs of metastatic disease, treated with curative intent.

Recruitment Participants are recruited through urology clinics and patient associations nationwide, as well as through social media such as Facebook and Instagram, and physical platforms such as bulletin boards and conferences. . receives standard care: standardized information about the importance of physical activity is included in the patients' care plan, which is offered to all prostate cancer patients. A Pilot Study A pilot study with five participants will be conducted before the intervention starts. The purpose of the pilot study is to test the yoga program. The pilot study will be evaluated through focus groups and individual interviews.

Data Collection Data is collected at baseline, within two months of diagnosis, after 3 and 6 months, and after 1 (and 2) years. An overview of the data collection schedule is shown in Appendix 2a.

Instruments for Patient-Reported Outcome Measures

  • The Perceived Stress Scale measures general stress and coping capacity. The instrument is validated in a Swedish population and has 14 questions. Response options are: almost never, sometimes, fairly often, or very often. The higher the score, the greater the reported stress.
  • EORTC-QLQ30 and the prostate cancer module measure health-related quality of life (HRQoL), consisting of 30 questions grouped into six scales: global health status, physical function, role function, emotional function, cognitive function, and social function. The prostate cancer module consists of 25 additional prostate cancer-specific questions.
  • EuroQol-5D is a generic standardized instrument for measuring health-related quality of life, which is the basis for the health economic calculation. It includes 5 questions. The The Expanded Prostate Cancer Index Composite questionnaire with 26 questions developed to measure the quality of life in patients with prostate cancer and previously used in Sweden .

Additional Data Collection Basic data: Age, gender, marital status, occupation, sick leave, phone number, email address, postal address, yoga experience.

Disease-related data: Diagnosis date, planned treatment, previous illnesses (comorbidity according to Charlson comorbidity index). Other: Changes in treatment and additional leaves

Blood Pressure Measurement Home blood pressure measurement will be done wit.h the OMROM blood pressure monitor (Blood pressure monitor from Omron - Best in test Omron (omron-sverige.se)) sent to study participants and kept if the person completes the data collection. Home blood pressure measurement is a reliable method used in Region Örebro County and eliminates the suspicion of white coat effect, i.e., stress during medical visits. Research participants are expected to check their blood pressure morning and evening every day for a week at 4 occasions: inclusion week, after 3, 6, and 12 months. An average value will then be calculated. At least 4 days of measurements will be accepted. Instructions for blood pressure measurement will be:

  • Sit and rest for 5 minutes
  • Measure blood pressure sitting with the arm resting on a table.
  • Measure morning and evening, two measurements with 1-2 minutes interval
  • Register blood pressure through the email you received

Yoga Activity All study participants (both control and intervention) register how much yoga they have practiced each week through a digital survey. Medical and other clinical data: will be collected from medical records and from the Information Network for Cancer (INCA) regarding treatment, dose intensity, toxicity, and side effects according to NCI-CTC 4.0, as well as time to relapse and survival.

Data Storage Electronic data storage: All collected data is handled according to Region Örebro County's routines for research data and the information management plan for research documents. Collected data is stored pseudonymized on a dedicated storage area for research data, FoU Drive, which is adapted to requirements for handling research data containing sensitive personal information. FoU Drive is located in Region Örebro County's own data center and is part of a central file server solution with redundancy, backup, and logging according to the region's routines. Data collection for surveys is done electronically through SmartTrial, an electronic support system for collecting research data in clinical studies. The database is provided by Region Örebro County and the security in the system is compliant with regulations for storing sensitive data. Regular backups are made to secure data. Logging into all levels of the system requires two passwords. Participants need a login to register their responses. SmartTrial sends text messages and emails to remind participants to log in and complete surveys. Participants who prefer paper surveys will receive them by mail along with a prepaid return envelope. Paper data will be stored at the research center where only the research team has access to the data.

Health Economic Assessment Health economic assessment will be conducted from both a healthcare perspective and a societal perspective. Cost-effectiveness will be presented as the incremental cost per quality-adjusted life year (QALY), but also as a probability of cost-effectiveness compared to standard care. The main components of the analysis are additional costs or savings of interventions and changes in QALY. Savings can be reduced sick leave (less production losses) or healthcare consumption. QALY will be estimated using the EQ5D-5L instrument, sick leave time collected through questionnaires to participants, and healthcare consumption will be retrieved from patient records.

Experience of Internet-Based Yoga The experience of participating in the internet-based yoga intervention will be described through a study with qualitative methods where 15-20 patients are interviewed about their experience of participating in a web-based yoga intervention. Interview questions: Main question: How has it been to participate in a yoga class online? Complementary questions: What have you experienced as positive? What have you experienced as negative? How have you experienced the group practicing yoga simultaneously? How has your stress level been affected by yoga? The interviews will be transcribed verbatim and then analyzed with qualitative content analysis.

Intervention Fidelity Adherence to the project's method is regularly monitored during the study. The intervention responsible researcher has regular contact with the instructors and ensures that the program is followed. The methodology for data collection has been tested in the previous study Digiyogacare, which included women operated for breast cancer 26.

All yoga instructors have more than 300 hours of experience as yoga instructors and undergo training that includes study design, diagnosis, yoga program with possible adaptations.

Monitoring Side Effects and Dropouts Patients are informed to report any side effects and, if possible, the reasons for not completing the study will be recorded and later presented.

Significance for the Research Field Previous research has shown that live yoga for prostate cancer has a positive effect on fatigue, urinary and sexual function, and improved quality of life. There are few studies in the area, and it is unclear if the same effects can be achieved with digital yoga. Digiyoga-P is a randomized controlled study designed to determine if digital yoga is effective rehabilitation for the patient group. The methodology with digital yoga has previously been tested and refined by parts of the research team through a study of another diagnosis group, women operated for breast cancer in the research project Digiyogacare: Digitally distributed Yoga Intervention in Breast Cancer Rehabilitation 26. The preliminary analysis shows good results, and the project's infrastructure is well established and can largely be used in a prostate cancer context. Now the yoga intervention is adapted to the prostate cancer-related issues, including pelvic floor strengthening movements. The knowledge gap that the project fills is: What effect does digital yoga have for men diagnosed and treated with prostate cancer? Does it affect stress, urinary incontinence, blood pressure, and quality of life, and is any effect lasting? Is internet-based yoga cost-effective? How feasible is it, and how do participants perceive internet-based yoga? Do the intervention group continue practicing yoga even after the intervention ends?

Patient Benefit Common issues associated with prostate cancer are stress, bowel and urinary problems, sexual issues, and reduced quality of life. These problems can be alleviated with proper rehabilitation. Having to travel to the hospital for rehabilitation reduces accessibility for patients living far from the hospital. It can also be overwhelming to travel for treatments and rehabilitation. This study investigates whether internet-based yoga is a feasible form of rehabilitation that can contribute to equal rehabilitation regardless of the place of residence. Yoga for men has become increasingly relevant and media-covered in recent years, and therefore we believe it will be an attractive rehabilitation for men treated for prostate cancer. If side effects of diagnosis and treatment can be alleviated for the large group of prostate cancer patients, well-being can increase, and the pressure on healthcare can be reduced.

Being tested
Digital yoga intervention
Keywords
RCT, rehabilitation, yoga, Digital, prostate cancer
Medical subject headings
Prostatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Digital yoga interventionOther

    Digital yoga intervention

Study groups in NCT07158138
Study groupRoleWhat they receive
Intervention groupExperimentalRecieves a digital yoga intervention
Receives: Other: Digital yoga intervention
ControllgroupNo interventionRecieves usual care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Does internet-based yoga have any effect on stress compared to standard care?

    • The Perceived Stress Scale (PSS)20 measures general stress and coping capacity. The instrument is validated in a Swedish population and has 14 questions. Response options are: almost never, sometimes, fairly often, or very often. The higher the score, the greater the reported stress.

    Measured: From enrollment to 12 months

  2. Stress

    The Perceived Stress Scale (PSS)20 measures general stress and coping capacity. The instrument is validated in a Swedish population and has 14 questions. Response options are: almost never, sometimes, fairly often, or very often. The higher the score, the greater the reported stress.

    Measured: From enrollment to 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Sep 2025
  2. Study start10 Jan 2026 (estimated)
  3. Primary completion10 Jan 2028 (estimated)
  4. Study completion10 Jan 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
The study is a randomized controlled multicenter study, where participants are randomized to an internet-based yoga intervention or a control group.
Masking
None (open label)
Enrolment
220 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07158138
Sponsor's protocol ID
Dnr 2025-02611-01
Acronym
Digiyoga-P
Status last verified
Aug 2025
First submitted
28 Aug 2025
Last updated
5 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Digital yoga intervention in people with Prostate Cancer Patients, run by Region Örebro County at 1 site in Sweden.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 5 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Emma Ohlsson-Nevo, A. professor (+460704366788, emma.ohlsson-nevo@regionorebrolan.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Does internet-based yoga have any effect on stress compared to standard care? (time frame: From enrollment to 12 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Sep 2025.

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