Validation of Walking and Remembering Test

March 4, 2025 updated by: Emre Şenocak

A Study to Assess The Balance Using Remote Access Method - Walking and Remembering Test Validation

In this study, the usability of the Walking and Remembering Test will be examined using the remote interview method. The study will be carried out with a single group. First, the WART test will be performed face-to-face at Marmara University Biomechanics Laboratory. The second evaluation will be carried out using a remote method. From the participants;

  • He/she will first be asked to walk freely within a line that is 8 meters long and 19 cm wide. Later;
  • He will be asked to walk once at average speed and three times as fast as possible in the same line. Later;
  • The participant is given a Counting Test. This test includes number sequences from 4 digits to 9 digits. Participants are told these number strings and asked to repeat them with the same speed and tone of voice. The longest sequence of numbers is recorded. Later;
  • The participant is walked on the same line again and asked to repeat the longest number sequence he remembers and the test is completed. Cognitive performance with the counting test reflects walking speed during 4 walks, and the number of incorrect steps reflects walking performance.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

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

      • İstanbul, Turkey, 34840
        • Marmara University, Department of Physiotherapy and Rehabilitation, Biomechanics and Performance Analysis Laboratory

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Having any known psychological, vestibular and neurological diseases,
  • No major or minor hip, knee or ankle injuries,
  • Not showing osteoarticular or muscle traumas that prevent upright posture and ambulation,
  • Not taking medications that affect posture, such as vestibular apparatus sedatives, antidepressants or anxiolytics,
  • Not complaining of dizziness or vertigo,
  • Being between the ages of 18-30.

Exclusion Criteria:

  • Individuals with untreated visual impairment,
  • Epilepsy, postural dizziness or hypotension,
  • Individuals with dependent ambulation,
  • Individuals with any disease that affects balance,
  • Those with cancer or fibromyalgia.

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

  • Primary Purpose: Screening
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Walking and Remembering Group
Only Walking and Remembering Test will be applied to the group.
Only Walking and Remembering Test will be applied to the group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Walking and Remembering Test (WART)
Time Frame: Baseline of the study (Face-to-Face)
WART is a clinical measure of dual-task ability involving individual and simultaneous motor and cognitive task performance. In the test, walking and memory are observed independently and under dual-task conditions.
Baseline of the study (Face-to-Face)
Walking and Remembering Test (WART)
Time Frame: First day after the Baseline Assessment (Remote Assessment)
WART is a clinical measure of dual-task ability involving individual and simultaneous motor and cognitive task performance. In the test, walking and memory are observed independently and under dual-task conditions.
First day after the Baseline Assessment (Remote Assessment)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Demographic Data Form
Time Frame: Baseline of the study
This form was created by researchers and it consist of personal informations such as gender, dominant extremity, history of sport, age, body mass index
Baseline of the study

Collaborators and Investigators

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

Sponsor

Investigators

  • Study Chair: Aysel Yildiz Ozer, Professor, Marmara University
  • Study Chair: Semra Oğuz, Associate Professor, Marmara University
  • Study Chair: Gökçe Kartal, MSc, Marmara 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)

July 29, 2024

Primary Completion (Actual)

February 28, 2025

Study Completion (Actual)

February 28, 2025

Study Registration Dates

First Submitted

August 29, 2024

First Submitted That Met QC Criteria

August 29, 2024

First Posted (Actual)

August 30, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 4, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 25.07.2024/112

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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