Spanish Validation Frustration Discomfort Scale

June 17, 2020 updated by: Universitat Jaume I

Spanish Validation of the Frustration Discomfort Scale

This is an observational study aimed at validating the Frustration Discomfort Scale (Harrington, 2005). A back-translation process was followed to obtain a translated version of the scale, which was refined after a discussion with several clinicians.

Study Overview

Status

Completed

Detailed Description

In the study, the Spanish adaptation of the Frustration Discomfort Scale will be disseminated with an online questionnaire using the Qualtrics platform. Additional questionnaires to explore the validity of the adapted scale will also be administered. Participants who complete the questionnaires and provide a valid ID number will enter a participate in a raffle to win an Amazon coupon of 40 euros. Ten coupons will be offered in total amongst participants.

Study Type

Observational

Enrollment (Actual)

1513

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Castellón De La Plana, Spain
        • Faculty of Psycholoy. Jaume I University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

This protocol will be disseminated globally to the population in Spain with no restriction. The maximum efforts will be made to disseminate the study to a wide range of individuals

Description

Inclusion Criteria:

  • Being over 18 years of age
  • Signs the informed consent
  • Can read and understand Spanish
  • Has access to a computer, a tablet or a smartphone with an internet connection

Exclusion Criteria:

  • Being younger than 18 years of age
  • Does not sign the informed consent
  • Cannot read or understand Spanish
  • Does not have access to a computer, a tablet or a smartphone with an internet connection

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Frustration Discomfort Scale
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This is a measure of frustration intolerance. The original English version has been translated using a back-translation method and discussions about item have been made with clinicians with expertise in the field. The scale has 28 items that are gouped in 4 subscales. Items have a 1-to-5 response scale ranging from "nothing" to "a lot"
The measure will be administered 1 day once only together with the remaining measures

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rosenberg self-esteem scale
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This scale of self-esteem has 10 items with responses ranging from 1 (completely agree) to 4 (completely disagree). This measure will be used for concurrent criterion validity analyses
The measure will be administered 1 day once only together with the remaining measures
Satisfaction with life scale
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This 5-item scale measures an individual's satisfaction with life using response options ranging from 1 (completely disagree) to 5 (completely agree). This measure will be used for concurrent criterion validity analyses
The measure will be administered 1 day once only together with the remaining measures
Acceptance and action questionnaire - II
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This 7-item scale measures acceptance of difficult experiences using a 7-point response scale (1= never true; 7=always true). This measure will be used for construct validity analyses
The measure will be administered 1 day once only together with the remaining measures
STAXI - 2 (trait anger scale only)
Time Frame: The measure will be administered 1 day once only together with the remaining measures
The trait anger scale of the STAXI-2, which has 10 items, will be used to evaluate trait anger. The responses in the scale range from 1="not at all" to 4="very much". This measure will be used for concurrent criterion validity analyses
The measure will be administered 1 day once only together with the remaining measures
Irrational Procrastination Scale
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This 9-item scale will be administered to measure perceived procrastination. Items in the scale have a 5-point range (1=does not describe me at all; 5=decribes me completely). This measure will be used for concurrent criterion validity analyses
The measure will be administered 1 day once only together with the remaining measures
Trait Injustice Experiences Questionnare
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This measure of perceived trait injustice beliefs has 12 items, with responses ranging from 0="never" to 4="always". This measure will be used for construct validity analyses
The measure will be administered 1 day once only together with the remaining measures
European version of the Perceived Stress Scale
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This 10-item measure of perceived stress will be used for concurrent criterion validity analyses. Responses in the scale range from 0="never" to 4="very frequently"
The measure will be administered 1 day once only together with the remaining measures
Patient Health Questionnaire
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This 10-item measure of depressive symptoms will be used for concurrent criterion validity analyses. Response scales range from 0="None of the days" to 3="Almost all days"
The measure will be administered 1 day once only together with the remaining measures
General Anxiety Disorder scale
Time Frame: The measure will be administered 1 day once only together with the remaining measures
This 7-item measure of anxiety symptoms will be used for concurrent criterion validity analyses. Response scales range from 0="None of the days" to 3="Almost all days"
The measure will be administered 1 day once only together with the remaining measures
General Attitudes and Beliefs Scale - reduced
Time Frame: The measure will be administered 1 day once only together with the remaining measures
A shortened, 12-item version of the General Attitudes and Beliefs Scale will be administered. This measure will be used for concurrent criterion validity analyses. Responses in the scale have a 1-5 range (1="completely disagree"; 5="completely agree")
The measure will be administered 1 day once only together with the remaining measures

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 10, 2020

Primary Completion (Actual)

May 30, 2020

Study Completion (Actual)

May 30, 2020

Study Registration Dates

First Submitted

January 20, 2020

First Submitted That Met QC Criteria

January 22, 2020

First Posted (Actual)

January 23, 2020

Study Record Updates

Last Update Posted (Actual)

June 18, 2020

Last Update Submitted That Met QC Criteria

June 17, 2020

Last Verified

May 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • FrustrationUJI

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Only the main PI will have access to the data.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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