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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04728776
Other study ID # 293
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 6, 2017
Est. completion date February 7, 2020

Study information

Verified date January 2021
Source University of Lahore
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

BACKGROUND Knowledge about the perceived impact of stroke on survivors' lives is still scarce in Pakistan due to the lack of translated and culturally adapted self-rating scales. The stroke impact scale is a comprehensive self-reported outcome measure designed to assess the quality of life following the stroke. Although the psychometric properties of SIS found to be superior to the conventional generic quality of life scales, it has not been translated and tested in Pakistan. OBJECTIVE To translate and cross-culturally validate the Urdu version of stroke impact scale 3.0 for Pakistan MATERIAL AND METHODS Established guidelines were followed for translation and adaption of the Stroke impact scale 3.0. A prospective cohort of 116 patients with mild to moderate stroke self-reported their recovery on the Urdu version of SIS 3.0. The patients were concurrently evaluated on the established scales to assess the validity using the Spearman correlation coefficient. ANOVA was used to determine the discriminant validity. Ninety patients were consecutively re-evaluated to determine the test-retest reliability, precision, minimal detectable change (MCD) and clinically minimally important difference. The coefficients of ICC, Cronbach's alpha, and weighted kappa were calculated to establish the stability and consistency of the scale. The receiver operating curve was used to estimate the MCID of SIS-16 using global rating scale as an anchor. KEYWORDS: Stroke, Stroke Impact Scale, Outcome Measures, Quality of Life


Recruitment information / eligibility

Status Completed
Enrollment 116
Est. completion date February 7, 2020
Est. primary completion date February 7, 2020
Accepts healthy volunteers No
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with acute, subacute or chronic stroke - Patients with hemorrhagic or ischemic or recurrent stroke attack - Age of patients between 50-80 - Ability to read and write Urdu with minimum education to 5th grade Exclusion Criteria: - Patients with severe neurological comorbidities - Patients having communication difficulties, such as patients with global aphasia or reduced consciousness.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Pakistan The University Of Lahore Teaching Hospital Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
University of Lahore

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Other Hospital Anxiety and Depression Scale, "Change" is being assessed The Hospital Anxiety and Depression Scale is 14 items scale for assessment of anxiety and depression. Scale consists of 7 items for depression and 7 items for depression and each item scored from 0 (no problem) to 3 (severe problem). Scores on individual items can be summed to calculate a score for anxiety and for depression and higher score is indicative of more depression and anxiety. Score of each sub scale varies from 0-21, where 0-7 means normal, 8-10 means mild, 11-14 means moderate, 15-21 means sever disorder. Day 1, A week after the first assessment, at discharge upto 12 week
Primary Stroke Impact Scale 3.0 "Change" is being assessed A 59-item self-reported scale with 8 domains, scores of each domain range from 0 to 100, and higher scores indicate a better health-related quality of life Day 1, A week after the first assessment
Primary Stroke Impact Scale-16 "Change" is being assessed It consists of 16 items of 4 physical function. Its score varies from 0 to 100 and higher score indicates more functioning of the patient Day 1, A week after the first assessment and at discharge upto 12 weeks
Secondary Short-form 36, "Change" is being assessed SF-36 is a generic HRQoL measure that includes 8 domains. Scores for each domain range from 0 to 100, and higher values indicate better function. Day 1, A week after the first assessment
Secondary Barthel Index, "Change" is being assessed The Barthel Index used to evaluate activities of daily living in stroke patients measures and measures 10 basic aspects of activities of daily living related to self-care and mobility: control of bowels and bladder, grooming, toilet use, feeding, transfer, mobility, dressing, stairs, and bathing. Its score ranges from 0 to 100, and lower scores indicate greater dependency. Day 1, A week after the first assessment
Secondary Stroke Rehabilitation Assessment of Movement, "Change" is being assessed Composed of 30 items, score range from 0-100, measures physical function and higher score indicates more physical functioning of patient Day 1, A week after the first assessment
Secondary Modified Rivermead Mobility Index, "Change" is being assessed A 15-items scale with each item score range from 0 to 5. Its score varies from 0 to 100 and higher score indicates more functioning of the patient Day 1, A week after the first assessment
Secondary Global rating of change scale "Change" is being assessed Measures self-perceived change in health status and the main purpose is to quantify the extent to which a patient has improved or deteriorated over time. Score lower than 0 means patient has deteriorated and more than 0 means patient has improved. Its score varies from -7 to +7 at discharge up to 12 weeks only, Please note it simply ask the patient how much change he has experienced over the course of treatment period
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