Normative Data of Dynamic Gait Index and 5 Time Sit to Stand Test Among Elderly Population

December 6, 2022 updated by: Riphah International University

Normative Data of Dynamic Gait Index and 5 Time Sit to Stand Test Among Elderly Population and Correlation With Anthropometric Parameters

The goal of this observational study is to measure the normative data for dynamic gait index and 5 time sit to stand test in elderly population. This study aimed for to take normative measurement of dynamic gait index and five time sit to stand test among elderly population and to compare the preliminary values of above mentioned tests with age.

Study Overview

Status

Completed

Conditions

Detailed Description

Anthropometric factors affect the stability limits of the individual and can affect the motor strategies relating to balance control. The core elements of anthropometry are height, weight, body mass index (BMI), body circumferences (waist, hip, and limbs), and skin-fold thickness. Some anthropometric variables, such as body mass, are directly related to postural balance. Due to lack of normative data for dynamic gait index and five times sit to stand test in elderly population, this study aimed to formulate normative values for dynamic gait index and five times sit to stand test among elderly and correlation with anthropometric measures. Objectives: The objective of this study was to take normative measurement of dynamic gait index and five times sit to stand test among elderly population and to compare the preliminary values of above mentioned tests with age. All possible elder population was taken in current study to calculate the normative values of these two tests, five times STS to measure the ability to get up from a chair and DGI to record dynamic gait tasks in elder people

Study Type

Observational

Enrollment (Actual)

400

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

    • Punjab
      • Lahore, Punjab, Pakistan, 54600
        • Maria Idrees
      • Lahore, Punjab, Pakistan, 54600
        • Riphah International 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

43 years to 58 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Data was collected from old age home in Lahore. Sample size of 400 subjects was chosen.

Group 1: 45-50 years Group 2: 50-55 years Group 3: 55-60 years

Description

Inclusion Criteria:

  • 45-60 years elderly population.
  • Both male and female were included in given age group.
  • Older adults ambulate without a device or assistance.
  • Population who has no deformity will be included.

Exclusion Criteria:

  • Older adults who cannot ambulate were excluded
  • Pregnant females were excluded from this study
  • Population having any deformities was not included in this study.
  • Any participants suffering from malignancy, infection or taking anticoagulant therapy were also excluded.

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: Ecologic or Community
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dynamic Gait index
Time Frame: 8 weeks

8 functional walking tests are performed by the subject and marked out of three according to the lowest category which applies. 24 is the total individual score possible. Scores of 19 or less have been related to increase incidence of falls.

Equipment needed

Box (Shoebox), Cones (2), Stairs, 20' walkway, 15" wide

Completion Time

15 minutes

8 weeks
5 times sit to stand test
Time Frame: 8 weeks

The Five Times Sit to Stand Test measures one aspect of transfer skill. The test provides a method to quantify functional lower extremity strength and identify movement strategies a patient uses to complete transitional movements.

The equipment need in performing 5XSST test includes: Stopwatch and chair with straight back (43-45 cm, 17-18 inches high). Then the instruction is given by asking the test taker to sit on the chair by resting their back. Also, the test taker is instructed to fold their arms across their chest. Then the test taker should be instructed to do sit-to-stand five times, as quickly as possible, at the count of go and without their back or leg resting on the chair between the interval of repetition

8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sumera Azam, MS, Riphah International University

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)

August 20, 2021

Primary Completion (Actual)

November 26, 2021

Study Completion (Actual)

January 27, 2022

Study Registration Dates

First Submitted

October 21, 2022

First Submitted That Met QC Criteria

December 6, 2022

First Posted (Estimate)

December 15, 2022

Study Record Updates

Last Update Posted (Estimate)

December 15, 2022

Last Update Submitted That Met QC Criteria

December 6, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Semera

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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