Actively Recruiting
To Live Better After Breast Cancer Treatment
Led by Karolinska Institutet · Updated on 2024-06-24
40
Participants Needed
1
Research Sites
113 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The most common cancer among women in Sweden is breast cancer. Advances in treatment have improved survival, but these advances have come at a steep price since most treatments impose substantial morbidity and burden on patients and their families. 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 and person-centered care intervention in primary healthcare for six months during the first year after primary treatment for breast cancer, assisted by digital technology and compare it to standard care only. The intervention consists of symptom reporting and management in an app in combination with health dialogues with a study-specific nurse at the Primary healthcare centre.
CONDITIONS
Official Title
To Live Better After Breast Cancer Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with breast cancer at the end of curative treatment
- Able to read and understand Swedish
- Considered physically, psychologically, and cognitively able to participate in the study
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
Research Team
K
Kristina Rooth, MSc
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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