The Mere-measurement Effect of Patient-reported Outcomes

Recruiting N/A Interventional Study
Measurement, Psychological Stress Speech Disorders Assessment, Self
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
170 (estimated)
Sponsor
Medical University of Vienna · Other
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About This Trial
The use of patient-reported outcome (PROs) have become increasingly commonplace across many healthcare settings over the past two decades. The value of PROs is now acknowledged by healthcare providers and patients alike. However, to date, little is known about the best practices for formulating PRO measures (PROMS), but even more specifically, the effect had on the responding patients as a result …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: All patients will be required to have a qualifying disorder known to effect speech as identified below. Patients who meet the eligibility criteria will be invited to participate in the study by the researchers. Eligibility will be assessed prior to enrolment recruitment screenin…
Contacts

Preston Long, PhD

+43 (0)1 40400-66100

preston.long@meduniwien.ac.at

CONTACT