- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04238325
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
Conditions
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.
Sponsor
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.
Clinical Trials on General Population, no Specific Condition
-
Charite University, Berlin, GermanyRecruitingGeneral Population (no Specific Condition or Disease)Germany
-
NYU Langone HealthNew York City Health and Hospitals CorporationCompleted
-
The University of Texas Health Science Center,...CompletedPediatric Endotracheal Intubation (no Specific Condition)United States
-
Assistance Publique - Hôpitaux de ParisCompletedthe Study Focus on no Specific ConditionFrance
-
Assistance Publique - Hôpitaux de ParisWithdrawnThe Study Focus on no Specific ConditionFrance
-
Assistance Publique - Hôpitaux de ParisUnknownThe Study Focus on no Specific ConditionFrance
-
Assistance Publique - Hôpitaux de ParisCompletedThe Study Focus on no Specific ConditionFrance
-
Assistance Publique - Hôpitaux de ParisWithdrawnThe Study Focus on no Specific ConditionFrance
-
Assistance Publique - Hôpitaux de ParisWithdrawnThe Study Focus on no Specific ConditionFrance
-
Assistance Publique - Hôpitaux de ParisWithdrawnThe Study Focus on no Specific ConditionFrance