- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06604416
Forward and Backward Walking Exercise on Physical and Cognitive Functions
September 19, 2024 updated by: Hilal Denizoğlu Külli, Atlas University
Acute Effect of Forward and Backward Walking Exercise on Physical and Cognitive Functions
To investigate the acute effects of forward and backward walking exercise on physical functions such as static and dynamic balance and cognitive functions such as attention, concentration, memory, processing speed, visual structuring skills, calculation and orientation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study is planned to investigate the acute effects of forward and backward walking on physical functions such as static and dynamic balance and cognitive functions such as attention, concentration, memory, processing speed, visual structuring skills, calculation and orientation.
50 healthy individuals were randomly divided into three groups for the study.
The groups were divided into Backward Walking Exercise Group (GYE) (n=17), Forward Walking Exercise Group (FWE) (n=16) and Control Group (CG)(n=17).
Before treatment for all three groups; sociodemographic and clinical data with the sociodemographic information form, physical activity levels with the International Physical Activity Survey Short Form, pain severity with the Visual Analog Scale (VAS), fatigue levels with the Borg Scale, the person's selective attention capacity and skills, processing speed and general executive processing abilities.
Stroop Test with TBAG Form to evaluate executive functions such as working memory, complex attention, planning and set shifting, with Trail Making Test, evaluation of dynamic balance, neuromuscular control and movement asymmetries with Y-Balance Test, static balance, postural stability evaluation on One Leg It was evaluated with the Standing Test.
The GYE group completed a 25-minute backward walking exercise session, the FWE group completed a 25-minute forward walking exercise session, and the control group completed a 30-minute sitting rest between evaluation tests.
After the exercises, there were significant differences in parameters such as attention, processing speed, concentration and maintenance of attention, working memory, planning, static and dynamic balance, and in the comparison between groups, significant differences were found in static balance and postural control (p<0.05).
It was observed that individuals in the backward walking group showed better improvements in some parameters after walking.
However, these results need to be supported by future studies.
Study Type
Observational
Enrollment (Actual)
50
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
-
-
Kagıthane
-
Istanbul, Kagıthane, Turkey
- Istanbul Atlas 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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Healthy university students aged 18-25 years were included in the study, excluding physically active individuals according to the International Physical Activity Scale Short Form.
Description
Inclusion Criteria:
- To be between the ages of 18-25,
- To be able to communicate verbally and in written Turkish,
- Not complaining of pain in any part of the body during physical activity,
- Performing a normal walking pattern without compensatory movements.
Exclusion Criteria:
- Participants participating in a routine exercise program
- History of upper or lower extremity pathology or injury in the last 6 months
- Diagnosed neurological disease
- Diagnosed cognitive impairment
- Having a diagnosed orthopedic disease
- Using a walking aid
- Inadequate cardiovascular fitness
- Dyspnea on exertion
- Contraindication to walking
- Receiving medical treatment that causes imbalance.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Backward walking exercise group
Healthy subjects aged 18-25 years were included in the study.
Cognitive and physical function assessments were performed face-to-face by a physiotherapist before and after backward walking exercise.
In addition, assessments during the exercise were performed by the same physiotherapist.
Assessments were made immediately before and immediately after the walking exercise.
All assessments were supervised by the physiotherapist.
|
The exercises consisted of a 5-minute warm-up on a treadmill followed by a 25-minute period of moderate backward walking.
|
|
Forward walking exercise group
Healthy subjects aged 18-25 years were included in the study.
Cognitive and physical function assessments were performed face-to-face by a physiotherapist before and after forward walking exercise.
In addition, assessments during the exercise were performed by the same physiotherapist.
Assessments were made immediately before and immediately after the walking exercise.
All assessments were supervised by the physiotherapist.
|
The exercises consisted of a 5-minute warm-up on a treadmill followed by a 25-minute period of moderate forward walking.
|
|
Control group
Participants did not perform any walking exercise.
Cognitive and physical function assessments were performed before and after the assessment tests, with 30 minutes of rest in between.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stroop Test TBAG Form
Time Frame: immediately pre and immediately post-exercise
|
Stroop Test TBAG Form was used to assess executive functions such as attention, memory, concentration, visual structuring skills, computational working memory, planning, visual scanning ability.
|
immediately pre and immediately post-exercise
|
|
Trail Making Test
Time Frame: immediately pre and immediately post-exercise
|
The Trail Making Test was used to assess executive functions such as working memory, complex attention, planning and set switching, visual-spatial processing and motor abilities.
The Trail Making Test consists of two parts, A and B.
|
immediately pre and immediately post-exercise
|
|
Y-Balance Test
Time Frame: immediately pre and immediately post-exercise
|
Y-Balance Test was used to evaluate dynamic balance, neuromuscular control and movement asymmetries.
|
immediately pre and immediately post-exercise
|
|
One Leg Standing Test
Time Frame: immediately pre and immediately post-exercise
|
One-leg Standing Test was used to assess static balance.
|
immediately pre and immediately post-exercise
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
International Physical Activity Questionnaire (IPAQ) Short Form
Time Frame: pre-assessments
|
The IPAQ Short Form was used to determine the physical activity levels of the participants.
|
pre-assessments
|
|
The Visual Analog Scale (VAS)
Time Frame: immediately pre and immediately post-exercise
|
This scale scores from 0 to 10. Higher scores indicate worse pain.
|
immediately pre and immediately post-exercise
|
|
Borg Fatigue Scale
Time Frame: immediately pre-exercises, during exercise and immediately post-exercise
|
It was used to determine the level of fatigue perceived by individuals before, during and after completing walking exercises.
|
immediately pre-exercises, during exercise and immediately post-exercise
|
|
Oxygen Saturation
Time Frame: immediately pre-exercises, during exercise and immediately post-exercise
|
In the study, saturation values were measured by pulse oximetry before, during and after exercise by the same physiotherapist.
|
immediately pre-exercises, during exercise and immediately post-exercise
|
|
Blood Pressure Assessment
Time Frame: immediately pre and immediately post-exercise
|
Blood pressure assessment was performed with a syphinguometer.
|
immediately pre and immediately post-exercise
|
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)
November 7, 2023
Primary Completion (Actual)
December 15, 2023
Study Completion (Actual)
February 1, 2024
Study Registration Dates
First Submitted
September 17, 2024
First Submitted That Met QC Criteria
September 17, 2024
First Posted (Actual)
September 19, 2024
Study Record Updates
Last Update Posted (Actual)
September 20, 2024
Last Update Submitted That Met QC Criteria
September 19, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- edaserenkarakaya
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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