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Reliability of the Incremental Shuttle Walk Test in University Students

Completed
Conditions
Incremental Shuttle Walk Test
Registration Number
NCT06638281
Lead Sponsor
Siirt University
Brief Summary

The aim of this study is to evaluate the inter-rater and intra-rater reliability of the incremental shuttle walk test in university students.

Detailed Description

The incremental shuttle walk test (ISWT) is a valid and reliable field test developed to evaluate functional exercise capacity. This test requires the participant to walk up and down a 10 m course marked by two cones placed 9 m apart. The walking speed, determined by an audio signal, is slow at first, but gradually increases every minute.

Although validity and reliability studies have been conducted in different disease groups and healthy populations, there is no study evaluating the inter-rater reliability of the incremental shuttle walk test in healthy individuals. Our research aims to evaluate the inter-rater and intra-rater reliability of the incremental shuttle walk test in university students.For this purpose, undergraduate nursing students will be included in our research.ISWT will be administered to students by two different researchers on the same day. For test-retest reliability the ISWT will be administered again by the same researchers on a different day (retest).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
49
Inclusion Criteria
  • Being a student of Siirt University Faculty of Health Sciences, Nursing Department
  • Being between the ages of 18-26
  • Understanding and speaking Turkish
Exclusion Criteria
  • Having a systemic, orthopedic or neurological disease
  • Participant wishes to withdraw from the study

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incremental Shuttle Walk Test ResultsAt baseline and within 2-7 days after first assessment

The number of completed shuttles will be recorded, and the total incremental shuttle walk distance (ISWD) will be calculated. Heart rate (HR), arterial blood pressure, saturation, perceived dyspnea, and fatigue according to the modified Borg scale will be assessed before, at the end of the test, and after a 5-min recovery.

Secondary Outcome Measures
NameTimeMethod
AgeBaseline

Age in years

WeightBaseline

Weight (kg)

HeightBaseline

Height (m)

Smoking StatusBaseline

Smoking status will be recorded

Trial Locations

Locations (1)

Siirt University

🇹🇷

Siirt, Turkey

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