Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
NCT05100121

To Live Better After Prostate Cancer Treatment:

Led by Karolinska Institutet · Updated on 2024-09-19

40

Participants Needed

1

Research Sites

114 weeks

Total Duration

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AI-Summary

What this Trial Is About

It is evident that patients receiving treatment for cancer have symptoms that often are undetected. Furthermore, many survivors from cancer have ongoing poor health and well-being and long-term rehabilitation and support should not be neglected to prevent recurrence and increase survival. There are good reasons to believe that routine collection of relevant patient-reported symptoms facilitates person-centered care where the patient is a participatory member of the team. This study aims to pilot-test a supportive intervention in primary care for six months during the first year after primary treatment for prostate cancer in primary care and compare it to standard care only. The intervention consists of symptom reporting and self-management in an app in combination with health dialogues with a study-specific nurse at a primary care centre.

CONDITIONS

Official Title

To Live Better After Prostate Cancer Treatment:

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with prostate cancer at the end of curative treatment
  • Able to read and understand Swedish
  • Considered physically, psychologically, and cognitively able to participate in the study
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Health Care Services Stockholm County (SLSO)

Stockholm, Sweden

Actively Recruiting

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Research Team

N

Nazmije Kelmendi, PHDstudent

CONTACT

A

Ann Langius-Eklöf, Professor

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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