- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04713839
Adult Sensory Processing Scale (ASPS) Version of Turkish (ASPS)
Cross-cultural Adaptation, Reliability, and Validity of Turkish Adult Sensory Processing Scale (ASPS)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The current study comprises three parts: cross-cultural adaptation, piloting, and examination of psychometric properties of the ASPS-T. The researcher contacted the developers of the original ASPS and received written permission from the authors to translate it into Turkish. This study was conducted by the Helsinki Declaration and Uskudar University. Clinical Research Ethical Board approved the study. After receiving both written and oral information about the project, all the study participants provided a signed consent form.
Phase 1: The cross-cultural adaptation process Translating the Turkish version of ASPS and the cross-cultural adaptation procedure was carried out under the guidance of Beaton et al. Translation from English to Turkish was performed by two therapists whose mother tongue is Turkish, also have fluent in English. Each of the translations was reviewed by three therapists, after the consensus on the final version, it was turned down by two native English-speaking translators. The final version was compared with the original version to reveal any inconsistencies; no discrepancies were observed. During the translation phase, minimal adjust were made to address linguistic.
Phase 2: Piloting process A pre-assessment was made with a pilot study to explore ASPS-Turkish's cultural harmony. The translated questionnaire was completed by 20 participants to identify any items that were not coherent. Four participants stated that they could not understand the meaning of avoid-kaçınmak, so investigators suggested yaşamamak, and this was accepted by participants. Three participants could not respond to the first item on factor 10, because participants had not traveled by boat or rides before, so that, investigators added the phrase "all types of vehicles" was added to the sentence. All the authors meet to compare the ASPS-T with the original version and assess its suitability after the minimal change, concluding that the current correction did not cause any loss of the meaning of the word. After the changes, pilot study participants evaluated the intelligibility of the scale with a 1 to 5 Likert scale, and confirm the clearness unanimously of them. Therefore, the final version of the ASPS-T which has minor changes was the best representation of the original, and each item was found to be suitable for Turkish patients. The pilot study participants were not included in the sample. After cultural equivalence had been achieved, 405 healthy individuals aged 18 and over were asked to complete the ASPS questionnaire.
Phase 3: Analysis of psychometric properties Exploratory and Confirmatory Factor Analysis (EFA and CFA) were used to measure the construct validity of the instrument, and test-retest analysis (interclass correlation coefficient) and Cronbach's alpha were used to evaluate the reliability of the instrument.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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State
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Istanbul, State, Turkey, 34662
- Uskudar University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- being aged 18-64 years, able to read and write, and being healthy
Exclusion Criteria:
- Who has a diagnosis of any disorders that preventing from completing the survey such as cancer or cognitive problems.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Participants
The participants were invited to the study, then each participant was asked to complete the self-report questionnaires.
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We didn't have an intervention program, we used two questionnaires to evaluate participants.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Adolescent/Adult Sensory Profile
Time Frame: 20 minutes
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Adult Sensory Processing Scale is designed to measure different behavioral response patterns (over-responding, under-responding, and sensory seeking) of specific sensory systems (tactile, proprioceptive, vestibular, auditory, and visual) that are indicative of sensory processing challenges.
Sensory responsiveness models related to different sensory systems in adults have been defined by over-responsiveness, under-responsiveness and sensory-seeking patterns similar to those in children.
A total of 11 factors and 48 items are defined and the number of questions for each factor is different.
All items are rated on a 5-point Likert scale with Never = 1, Rarely = 2, Sometimes = 3, Often = 4, and Always = 5.
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20 minutes
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Adolescent/Adult Sensory Profile
Time Frame: 18 minutes
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The AASP was developed build on Dunn's sensory processing model and is suitable for aged over 11 years.
It consists of 60 items and is used to evaluate individuals' sensory processing skills in daily life.
Each item is related to responses to sensory input through six different sensory factors that refer to everyday activities, including taste/smell, movement, vision, touch, processing, auditory processing, and activity level.
The responses of the participants' sensory stimuli are evaluated in four quadrants: low registration, sensory sensitivity, sensory avoiding, and sensory seeking.
The responses record on a Likert scale as almost always, often, sometimes, rarely, and almost never, and the scores of the related items are added to supply the score for each quadrant.
The tests to settle the validity and reliability of the AASP were completed by Ucgul et al.
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18 minutes
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: ORKUN ARAN, PHD, Hacettepe University
- Study Chair: SEDEF ŞAHİN, PHD, Hacettepe University
- Study Director: ZEYNEP BAHADIR AGCE, PHD, Uskudar University
Publications and helpful links
General Publications
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 61351342-193
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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