Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06443073

The Mere-measurement Effect of Patient-reported Outcomes

Led by Medical University of Vienna · Updated on 2025-05-14

170

Participants Needed

1

Research Sites

85 weeks

Total Duration

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AI-Summary

What this Trial Is About

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 of item word choice, emotional valence, or frequency of use. That is, 1) does the positive or negative wording of items affect the patient's perspective on the latent variable, 2) is there a degree of subliminal influence or measurement effects on their behaviour resulting from exposure to PROs, and finally, 3) is such an effect amplified with repeated exposure?

CONDITIONS

Official Title

The Mere-measurement Effect of Patient-reported Outcomes

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Strong English skills
  • Ability to use online technology to complete questionnaires
  • Diagnosis of one of the following speech disorders: Muscle tension dysphonia, Inducible laryngeal obstruction, Amyotrophic lateral sclerosis (ALS), Stroke or other brain injury/damage/trauma causing aphasia or dysarthria, Parkinson's disease
  • Patients can be located anywhere globally
  • Adults aged 18 and older
Not Eligible

You will not qualify if you...

  • Under the age of 18

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Preston Long

Vienna, Austria, 1020

Actively Recruiting

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Research Team

P

Preston Long, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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