Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06719206

Reduce Sedentary Behavior During Cancer Treatment - the RedSedCan Study

Led by Mälardalen University · Updated on 2026-01-30

172

Participants Needed

2

Research Sites

304 weeks

Total Duration

On this page

Sponsors

M

Mälardalen University

Lead Sponsor

R

Region Västmanland

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Reduce Sedentary Behavior During Cancer Treatment - the RedSedCan Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with breast, prostate, or colorectal cancer and planned for or recently started neo- or adjuvant treatment such as chemotherapy, radiotherapy, or endocrine treatment
  • Receiving treatment at hospitals in Uppsala or Västerås, Sweden
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Diagnosed with dementia
  • Diagnosed with severe psychiatric disease
  • Severe loss of vision or difficulty communicating
  • Unable to walk indoors independently, with or without a walking aid
  • Completed treatment for other cancer diseases less than 12 months ago or not recovered from previous cancer treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Akademiska sjukhuset

Uppsala, Sweden

Actively Recruiting

2

Västmanlands sjukhus

Västerås, Sweden

Actively Recruiting

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Research Team

P

Petra von Heideken Wågert, Professor

CONTACT

A

Anna Henriksson

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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