Supportive care for breast cancer survivors using digital technology
To Live Better After Breast Cancer Treatment - a Randomized Pilot Trial of a Supportive and Person-centered Care Intervention in Primary Healthcare
This study is testing a new mobile app that helps breast cancer survivors manage their symptoms and connect with healthcare providers to see if it improves their quality of life compared to regular care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Karolinska Institutet Academic / other |
| Locations | 1 site (Stockholm) |
| Trial ID | NCT06471452 on ClinicalTrials.gov |
What this trial studies
This study aims to pilot-test a supportive and person-centered care intervention for breast cancer survivors during the first year after primary treatment. It involves the use of a mobile application for symptom reporting and management, combined with health dialogues with healthcare providers. The intervention will be compared to standard care to assess its effectiveness in improving patient-reported outcomes and overall quality of life. The study focuses on addressing the ongoing health challenges faced by breast cancer survivors and enhancing their rehabilitation and support.
Who should consider this trial
Good fit: Ideal candidates are women who have completed curative treatment for breast cancer and can read and understand Swedish.
Not a fit: Patients who are not physically, psychologically, or cognitively able to participate in the study may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the quality of life and health outcomes for breast cancer survivors.
How similar studies have performed: Previous studies have shown promising results with similar approaches, indicating potential for improved symptom management and quality of life.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients with breast cancer at the end of curative treatment * able to read and understand Swedish * considered being physically, psychologically and cognitively able to participate in the study Exclusion Criteria: \-
Where this trial is running
Stockholm
- Health Care Services Stockholm County (SLSO) — Stockholm, Sweden (Recruiting)
Study contacts
- Principal investigator: Ann Langius-Eklöf, Professor — Karolinska Institutet
- Study coordinator: Kristina Rooth, MSc
- Email: kristina.rooth@ki.se
- Phone: 0046707526845
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.