Implementing PROMs and PREMs in Routine Clinical Care: Assessment of Requirements and Impact

Recruiting N/A Interventional Study
PROMs PREMs Implementation Research Impact Evaluation
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
1,440 (estimated)
Sponsor
Parc de Salut Mar · Other
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About This Trial
There has been increasing interest in the use of patient-reported outcomes and experience measures (PROMs and PREMs) in clinical practice; yet few empirical studies have been conducted to evaluate the usefulness of such implementation. Objective: To evaluate the efficacy of the implementation of PROMs and PREMs in routine clinical care for improving health outcomes and satisfaction with health ma…
Trial Locations
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Eligibility 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 acce…
Contacts

Olatz Garin, PhD

+34 636210255

ogarin@researchmar.net

CONTACT