Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

Reducing sitting time and increasing daily activity during cancer treatment

Official title: Reduce Sedentary Behavior During Cancer Treatment - the RedSedCan Study

Run by Mälardalen University · NCT06719206 · Data updated 2026-11-12

This project will try a digital self-management program plus physiotherapist support to help people with breast, prostate, or colorectal cancer who are starting neo- or adjuvant treatment sit less and feel better during and after treatment.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment210 (estimated)
SponsorMälardalen University
Academic / other
Drugs / interventionschemotherapy
Locations2 sites (Uppsala and 1 other locations)
StatusRecruiting
StartedMarch 1, 2025
Main results expectedDecember 31, 2029
Study endsDecember 31, 2030
Registry record updatedOctober 1, 2026
Trial IDNCT06719206 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with breast, prostate, or colorectal cancer who are planned for or recently started neo- or adjuvant treatment at participating hospitals in Uppsala or Västerås, who can walk independently and use digital tools, are the intended participants.

Probably not a fit

Patients with dementia, severe psychiatric disease, severe vision or communication impairments, inability to walk independently, or those recently treated for another cancer are excluded and unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multicenter randomized controlled study tests a digital self-management program developed with patients to reduce sedentary behavior during ongoing neo- or adjuvant treatment for breast, prostate, or colorectal cancer. Participants use existing goal-setting technology and receive physiotherapist support to choose activities that replace time spent sitting. The trial measures objectively recorded sedentary time, patient-reported well-being, and includes health-economic and climate-benefit analyses. Recruitment takes place at hospitals in Uppsala and Västerås, Sweden with short- and long-term follow-up.

Why it matters

Potential benefit: If effective, the intervention could help patients spend less time sitting during treatment, improve short-term well-being, and lower long-term risks such as treatment-related cardiovascular complications.

How similar studies have gone: Previous smaller trials and pilot studies suggest digital coaching and physiotherapist-supported programs can reduce sedentary time and improve quality of life in cancer patients, but large randomized multicenter evidence is still limited.

Who can join: the full rules

Show full inclusion / exclusion 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.

Where it's running

  • Akademiska sjukhuset
    Uppsala, Sweden
    Recruiting
  • Västmanlands sjukhus
    Västerås, Sweden
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.