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Clinical Trials in Sweden / NCT06719206
Recruiting Not applicable

Reduce Sedentary Behavior During Cancer Treatment - the RedSedCan Study

NCT06719206 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2025-03-01
Last updated
2026-10-01

Condition(s) studied

Breast CancerColorectal Cancer (CRC)Prostate CancerNeoadjuvant TherapyAdjuvant Therapy

Investigational drug(s) / intervention(s)

Digital self-management program

Digital self-management program: The program consists of commercially available technologies, e.g. applications including behavour change techniques for reducing sedentary behavior (SB) (i.e. self-monitorization of physical activity, reminders for breaking SB/doing physical activity, and providing feedback on physical activity/breaks from SB) and a webpage containing information and tips (provided in short videos and text) regarding how to reduce SB. The participants will be receive help with setting goals for reducing time spent in sedentary/being active and help with planning for what activities to do to replace time in sedentary. Participants will then have access to the webpage and download the application to their smartphones. Follow-up meetings with the physiotherapist (digital or physical) will be conducted after 2, 8 and 12 weeks after start of intervention.

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Akademiska sjukhuset Uppsala Sweden Recruiting
Västmanlands sjukhus Västerås Sweden Recruiting

More Mälardalen University trials in Sweden

Other trials for the same condition

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 NCT06719206 on ClinicalTrials.gov ↗ ← All trials in Sweden