- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05509205
Turkish Adaptation, Validity and Reliability of Pound Satisfaction Scale in Patients With Stroke After Stroke Rehabilitation
August 23, 2022 updated by: Emel Mete, Istanbul Medeniyet University
The aim of this study is to adapt the Pound Satisfaction Scale (PSS) to Turkish society in stroke patients and to make its validity and reliability in Turkish.
The PSS scale developed by Pound et al evaluates the patient's satisfaction with the received rehabilitation program and services received in stroke patients.
The PSS scale will be filled in face-to-face with volunteer participants who have received a stroke rehabilitation program and meet the inclusion criteria.
130 participants will be included in the study.
In order to assess the concurrent validity of the PSS, the SF-36 (short form) which evaluates the quality of life, and the Patient Satisfaction Scale in Physiotherapy (PSSP) which evaluates patient satisfaction will be used.
Scales will be repeated after 15 days to assess test-retest reliability.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The reliability and validity of the scale will begin with language equivalence and cultural adaptation.
The scale will be translated from English to Turkish by two people who are fluent in Turkish and English.
A single Turkish translation will be obtained from these two Turkish translations with a common opinion.
The scale, which has been translated into Turkish, will be translated into English by two other people who are fluent in Turkish and English.
The scale translated into English will be compared with the original.
If the developer of the scale approves the translation of the scale, participants will be recruited for the study.
In the pre-trial phase, a preassessment will be conducted with 15 participants to test the intelligibility of the scale.
Based on the results of the pre-test phase, the final version of PSS will be able to be modified.
The PSS scale will be filled in face-to-face with volunteer participants who have received a stroke rehabilitation program and meet the inclusion criteria.
130 participants will be included in the study.
In order to assess the concurrent validity of the PSS, the SF-36 (short form) which evaluates the quality of life, and the Patient Satisfaction Scale in Physiotherapy (PSSP) which evaluates patient satisfaction will be used.
Scales will be repeated after 15 days to assess test-retest reliability.
Study Type
Observational
Enrollment (Anticipated)
130
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
-
-
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Istanbul, Turkey, 34854
- Recruiting
- Emel Mete
-
Sub-Investigator:
- Zubeyir SARI, Professor
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-
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 to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Stroke patients who are treating with stroke rehabilitation
Description
Inclusion Criteria:
- To benefit from Physiotherapy and Rehabilitation services,
- Mini mental state examination (MMSE) score> 24
- Patients with stroke
- Native language being Turkish
Exclusion Criteria:
- Native language not being Turkish
- Patients with motor sequelae from other diseases and insufficient cognitive or educational level to complete the scale
- Mini mental state examination (MMSE) score < 24
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients with stroke
In this study 130 patients with stroke who are treating with stroke rehabilitation programs, will be included.
|
This study is about validation of the Pound Satisfaction Scale to Turkish.
The level of satisfaction with the rehabilitation service and treatment of 130 stroke patients undergoing stroke rehabilitation will be evaluated with the Pound satisfaction scale.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Personal Satisfaction
Time Frame: baseline
|
Personal Satisfaction will be assessed with Pound Satisfaction Scale (PSS).
The scale includes three sub-categories: "care and information given to the patient during treatment", "quantity and quality of treatment" and "Information and support provided to the patient and family after discharge".
PSS consists of 13 items in total.
Each item is scored ranging from 0 to 3 (0: Strongly disagree, 1: Disagree, 2: Agree, 3: Strongly agree).
The highest score is 39 points.
High scores indicate a high degree of satisfaction.
|
baseline
|
|
Patient satisfaction
Time Frame: baseline
|
Patient Satisfaction from physiotherapy will be assessed Patient Satisfaction Scale in Physiotherapy (PSSP).
PSSP consists of 14 items under four category subheadings of "treatment (5 items), admission (3items), logistics (4items) and global overall satisfaction (2 items)."
It is a 5-point Likert type scoring scale (1 = weak, 5 = perfect).
Total scores are calculated out of 100.
High scores indicate a high degree of satisfaction.
|
baseline
|
|
Life quality
Time Frame: baseline
|
Life quality will be assessed with SF-36 (short form).
SF-36 (short form) is a general quality of life scale that evaluates physical and mental health.
It consists of eight sub-dimensions and 36 items: Physical Function, Social Function, Physical Role Difficulty, Emotional Role Difficulty, Mental Health, Vitality (Energy), Pain and General Health.
Scores for each subscale are calculated separately.
It is scored from 0 to 100.
A score of 0 from the scale indicates poor health, and a score of 100 indicates good health.
|
baseline
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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)
March 2, 2022
Primary Completion (Anticipated)
August 30, 2022
Study Completion (Anticipated)
September 10, 2022
Study Registration Dates
First Submitted
August 18, 2022
First Submitted That Met QC Criteria
August 18, 2022
First Posted (Actual)
August 22, 2022
Study Record Updates
Last Update Posted (Actual)
August 26, 2022
Last Update Submitted That Met QC Criteria
August 23, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pound Satisfaction Scale
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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