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Developing and Validating Digital Affective Patient Experience/Outcome Measure (ETVa)

H

Helsinki University Central Hospital (HUCH)

Status

Unknown

Conditions

Affective; Reaction
Pregnancy Related
Validation Studies

Study type

Observational

Funder types

Other

Identifiers

NCT03337321
2329/2016

Details and patient eligibility

About

The aim of the research project is to develop and validate a new digital measure of affective patient experience in maternal care. In this validating study extensive collection of affective ratings of 195 emotion words is collected. Pregnant women at different gestational stages are asked to provide affective ratings of 195 emotion words in relation to the dimensions: pleasure, arousal, dominance. Based on these ratings population averages and properties of emotion words will be calculated. The measure will be developed in respect to the analysis of affective rating and supplementing data.

Full description

As there is an increasing demand for and interest in measures that take patient's emotions into account, this research project aims to develop and validate a new digital measure of affective patient-reported experience/outcome in maternal care.

In this validating study extensive collection of affective ratings of 195 emotion words will be collected. Pregnant women (N=1000) at different gestational stages are asked to provide affective ratings of 195 emotion words in relation to the dimensions: pleasure, arousal, dominance. This is done by using a visual Likert scale (Self-Assessment Manikin). The pregnant women participating in the research are also asked to answer to various questionnaires to identify patterns of personality, behavior and the state of health and well-being. Based on the affective ratings population averages and properties of emotion words will be calculated. The measure will be developed in respect to the analysis of affective ratings and supplementing data.

The research provides insights on how affective ratings could be connected to clinical indicators and patient experience.

Enrollment

1,000 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • ongoing pregnancy
  • attending maternal care in the Hospital District of Helsinki and Uusimaa
  • fluent in Finnish
  • access to mobile communication device

Exclusion Criteria: none

Trial design

1,000 participants in 1 patient group

ETvalid
Description:
Pregnant women attending maternal care services and having access to computational device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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