Using patient-reported outcomes and experiences in routine healthcare
Implementing PROMs and PREMs in Routine Clinical Care: Assessment of Requirements and Impact.
NA · Parc de Salut Mar · NCT06272552
This study is testing if using a smartphone app to collect feedback from patients about their health and experiences can improve care and satisfaction for adults with conditions like cancer or those having weight loss surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 1440 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Parc de Salut Mar (other) |
| Locations | 1 site (Barcelona, Catalonia) |
| Trial ID | NCT06272552 on ClinicalTrials.gov |
What this trial studies
This study evaluates the implementation of patient-reported outcomes (PROMs) and patient-reported experience measures (PREMs) in routine clinical care to assess their impact on health outcomes and patient satisfaction. It is a randomized control trial involving 1,440 adult patients with conditions such as breast cancer, prostate cancer, chronic kidney disease, or those undergoing bariatric surgery. Participants will complete PROMs and PREMs monthly via a smartphone app, with results shared during follow-up visits to enhance communication between patients and healthcare providers.
Who should consider this trial
Good fit: Ideal candidates are adult patients actively receiving treatment for breast cancer, prostate cancer, chronic kidney disease, or bariatric surgery who are fluent in Spanish and have access to the internet.
Not a fit: Patients under 18 years of age or those without access to the necessary technology may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved health outcomes and greater patient satisfaction in clinical settings.
How similar studies have performed: Other studies have shown promise in using PROMs and PREMs in clinical settings, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Being an active patient of the nephrology service, prostate cancer service, breast cancer service, or bariatric surgery service * In possession of an email account and having basic knowledge of how to manage emails * In possession of a smartphone, computer, or tablet with access to the Internet * Fluent and able to read in Spanish Exclusion Criteria: \- Under 18 years of age
Where this trial is running
Barcelona, Catalonia
- Hospital del Mar Reseach Institute — Barcelona, Catalonia, Spain (RECRUITING)
Study contacts
- Principal investigator: Olatz Garin, PhD — Hospital del Mar Research Institute
- Study coordinator: Olatz Garin, PhD
- Email: ogarin@researchmar.net
- Phone: +34 636210255
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.
Conditions: PROMs, PREMs, Implementation Research, Impact Evaluation, PRMs Implementation, Implementation evaluation, Impact evaluation, RCT