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Spanish Adaptation and Study of Reliability of the European Quality Questionnaire (EuroQ2)

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ClinicalTrials.gov Identifier: NCT02686970
Recruitment Status : Recruiting
First Posted : February 22, 2016
Last Update Posted : November 29, 2016
Sponsor:
Information provided by (Responsible Party):
Francisca Pérez-López, Corporacion Parc Tauli

Brief Summary:
The aim of this study is to adapt and validate to the Spanish the European Quality Questionnaire (EuroQ2) to evaluate families' experiences of quality of care for critically ill and dying patients in the ICU.

Condition or disease
Critical Illness

Detailed Description:
The aim of this study is to adapt and validate a Spanish-language version of the European Quality Questionnaire (EuroQ2). Using a forward-backward translation methodology, we will translate the EuroQ2 into Spanish and will evaluate its psychometric characteristics in a clinical sample of 200 family members responsible for making medical decisions for patients who are discharged from the ICU or who died in the ICU. Cronbach's alpha values, confirmatory factor analysis (CFA) will be evaluated in order to know the reliability, construct validity, and convergent validity.

Study Type : Observational
Estimated Enrollment : 200 participants
Time Perspective: Prospective
Official Title: Spanish Adaptation and Study of Reliability of the European Quality Questionnaire (EuroQ2)
Study Start Date : November 2016
Estimated Primary Completion Date : February 2017
Estimated Study Completion Date : June 2017



Primary Outcome Measures :
  1. European Quality Questionnaire (euroq2) [ Time Frame: 48 h after discharge of patients alive from ICU or 1 month after the death into ICU ]
    Opinions about Quality of care of ICU after the stay



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Family member or person responsible for patient decision making in the ICU
Criteria

Inclusion Criteria:

  • Family members of patients admitted to the ICU for 48 hours or more.
  • Family members responsible for patient decision making in the ICU who consent participate.

Exclusion Criteria:

  • Family members younger than 18 years,
  • Family members not able to read or write Spanish

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02686970


Contacts
Contact: Francisca Pérez-López, RN, MSc 34-937231010 ext 21152 fperez@tauli.cat
Contact: Francisca Pérez, RN, MSc 34-937231010 ext 21152 fperez@tauli.cat

Locations
Spain
Corporacion Parc Taulí Recruiting
Sabadell, Barcelona, Spain, 08208
Contact: Francisca Pérez, RN MSc    34-937231010 ext 21152    fperez@tauli.cat   
Sponsors and Collaborators
Corporacion Parc Tauli
Investigators
Principal Investigator: Francisca Pérez-López, RN, MSc Corporacion Parc Tauli

Publications of Results:
Other Publications:
Responsible Party: Francisca Pérez-López, RN, Corporacion Parc Tauli
ClinicalTrials.gov Identifier: NCT02686970     History of Changes
Other Study ID Numbers: CorporationPT
First Posted: February 22, 2016    Key Record Dates
Last Update Posted: November 29, 2016
Last Verified: November 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Francisca Pérez-López, Corporacion Parc Tauli:
Family
Quality
Validate
ICU

Additional relevant MeSH terms:
Critical Illness
Disease Attributes
Pathologic Processes