← Back to Clinical Trials
Recruiting NCT06719206

NCT06719206 Reduce Sedentary Behavior During Cancer Treatment - the RedSedCan Study

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06719206
Status Recruiting
Phase
Sponsor Mälardalen University
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 172 participants
Start Date 2025-03-01
Primary Completion 2029-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Digital self-management program

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 172 participants in total. It began in 2025-03-01 with a primary completion date of 2029-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Summary Reducing sedentary behavior during treatment is important to reduce the risk of future health problems in individuals undergoing cancer treatment. Therefore, the goal of this project is with a multicenter randomised controlled design investigate whether a digital support intervention during ongoing neo- or adjuvant cancer treatment for breast, prostate or colon cancer is effective in reducing sedentary lifestyle and improving well-being in the short and long term.

Eligibility Criteria

Inclusion Criteria: * Individuals diagnosed with breast, prostate, or colorectal cancer planned for or resently started neo- or adjuvant treatment (e.g. chemotherapy, radiotherapy, endocrine treatment) at the hospitals in Uppsala and Västerås, Sweden. Exclusion Criteria: * Individuals diagnosed with dementia. * Individuals diagnosed with severe psychiatric disease. * Individuals with severe loss of vision, or communicative ability. * Individuals who cannot walk independently indoors with or without a walking aid. * Individuals completed treatment for other cancer diseases less than 12 months ago or not recovered from previous cancer treatment.

Contact & Investigator

Central Contact

Petra von Heideken Wågert, Professor

✉ petra.heideken.wagert@mdu.se

📞 +46 (0)21-10 3188

Principal Investigator

Petra von Heideken Wågert, Professor

PRINCIPAL INVESTIGATOR

Mälardalen University

Frequently Asked Questions

Who can join the NCT06719206 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06719206 currently recruiting?

Yes, NCT06719206 is actively recruiting participants. Contact the research team at petra.heideken.wagert@mdu.se for enrollment information.

Where is the NCT06719206 trial being conducted?

This trial is being conducted at Uppsala, Sweden, Västerås, Sweden.

Who is sponsoring the NCT06719206 clinical trial?

NCT06719206 is sponsored by Mälardalen University. The principal investigator is Petra von Heideken Wågert, Professor at Mälardalen University. The trial plans to enroll 172 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology