- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06754579
Impact of High-Volume Upper Limb Training on Physical and Cognitive Outcomes
Effect of High-Volume Upper Extremity Exercises on Physical and Cognitive Performance in Sedentary Adults
Study Overview
Status
Conditions
Detailed Description
Engaging in regular, well-structured physical activities is a cornerstone of a healthy lifestyle and constitutes a lifelong habit essential for sustaining overall health and well-being. Such activities have been increasingly recognized for their vital role in preventing and managing a wide range of health conditions, emphasizing their importance for both physical and mental health (Martin, Richardson, Weiller, & Jackson, 2004). Conversely, a sedentary lifestyle has emerged as one of the most pressing public health challenges of the modern era, contributing significantly to the global burden of disease and highlighting the need for effective intervention strategies.
Among these strategies, high-intensity interval training (HIIT) has gained widespread attention for its efficacy in improving cardiovascular health. This has, in turn, sparked growing interest in understanding the broader impact of exercise intensity, particularly its effects on cognitive function. However, much of the existing research has concentrated on lower extremity exercises, such as those performed on treadmills or ergometers, leaving a significant gap in the understanding of the benefits of upper extremity exercises. The role of high-volume upper extremity exercise in enhancing both physical and cognitive performance remains underexplored, with current evidence presenting inconsistent and conflicting findings.
Notably, upper extremity motor function has been identified as a promising biomarker for cognitive impairment. Its assessment may provide critical insights into distinguishing healthy aging trajectories from pathological cognitive decline. This connection underscores the potential importance of upper extremity exercises as a tool for both physical and cognitive health maintenance in sedentary populations.
The present study aims to address these gaps by comparing the effects of high-volume and low-volume upper extremity exercise regimens on sedentary adults. Specifically, the research seeks to test the hypothesis that one of these exercise modalities may offer superior benefits in enhancing physical performance, cognitive performance, and overall cognitive function. By investigating these relationships, the study aims to contribute to the growing body of evidence on exercise-based interventions, offering novel insights into strategies for optimizing health outcomes in sedentary individuals.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Mersi̇n
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Tarsus, Mersi̇n, Turkey (Türkiye), 33400
- Recruiting
- Fatma kübra çekok
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Contact:
- Fatma K Çekok, PhD.
- Phone Number: 05434857545
- Email: kubracekok@tarsus.edu.tr
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Contact:
- Nurel Ertürk, PhD.
- Phone Number: 05434857545
- Email: nurelerturk@tarsus.edu.tr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Individuals aged between 18-50 years.
- Defined as engaging in less than 150 minutes of moderate-intensity physical activity per week
Exclusion Criteria:
- diagnosis of neurological, cardiovascular, musculoskeletal, or other systemic diseases that may affect physical activity or exercise capacity.
- diagnosed cognitive impairments or psychiatric disorders that could interfere with test participation.
- acute injuries or surgeries within the past six months that could restrict movement or participation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: High-Volume Upper Extremity Exercises Training
The High volume upper extremity protocol consists of a 5-min warm-up at 60%-70% of max HR using an arm ergometer, followed by four 4-min work sessions reaching 90%-95% of max W, followed by a 3-min active recovery period at 60% max W. The exercise session is terminated by a 5-min cool-down at 60%-70% max W. The total exercise duration will be 35 minutes.
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The group will be trained 3 days a week for a total of 8 weeks.
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|
Experimental: Low Volume Upper Extremity Exercises Training
Low volume upper extremity exercise training will be applied using an arm ergometer consisting of a 5-minute warm-up at 40% of max W, followed by 25 minutes of active training at 60-70% of max W and a 5-minute cool-down at 40% of max.
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The group will be trained 3 days a week for a total of 8 weeks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
International Physical Activity Questionnaire-Short Form (IFQQ-SF)
Time Frame: eight weeks
|
International Physical Activity Questionnaire-Short Form (IFQQ-SF): UFQ-SF was developed by Craig and colleagues to determine the physical activity levels of individuals between the ages of 15-65.
The short form is recommended more because the long form is boring and repetitive, so the "last 7 days" short form was used in our study.
The short form (7 questions) provides information on time spent in sitting, walking, moderate-intensity and vigorous activities.
The total score is expressed as one MET-min/week and is obtained by multiplying the number of days and minutes of walking, moderate-intensity and vigorous activity and the MET score.
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eight weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal Arm Exercise Capacity
Time Frame: Eight weeks
|
The arm ergometer test is a widely used method to evaluate maximal arm exercise capacity, requiring the involvement of chest, back, hip, and leg muscles for body stabilization.
This is particularly important as the test primarily targets a smaller muscle mass compared to bicycle ergometer testing.
For this study, the Monark 881E Rehab Trainer (MONARK 881E, Monark, Varberg, Sweden) arm ergometer will be employed.
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Eight weeks
|
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Stroop Test
Time Frame: Eight weeks
|
The Stroop Test utilized in this study is based on the Istanbul Medical Faculty (Çapa) Neuropsychology Laboratory adaptation of the Stroop Test form originally developed by Weintraub (2000).
Participants are instructed to name the colors of the small rectangles (red, blue, green) as quickly as possible, moving from left to right.
This stage is used to identify any visual or color perception impairments, such as color blindness.
If such deficiencies are detected, the test is discontinued.Stroop B (word reading): Participants are asked to read aloud the printed color names (red, blue, green) that are written in incompatible ink colors as quickly as possible.
Stroop C (Color-Word Interference).
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Eight weeks
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Reaction Time
Time Frame: Eight weeks
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The auditory and visual reaction times of sedentary individuals will be assessed using the Newtest 1000™ device (OY, Oulu, Finland).
This device is capable of delivering three types of stimuli and consists of two primary components designed for precise reaction time measurements.Following the familiarization trial, three measurements will be conducted for each type of stimulus (auditory and visual), and the reaction times will be recorded in milliseconds.
This protocol ensures the reliability of the data and accounts for variability in individual performance.
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Eight weeks
|
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Hole Type Steadiness Tester
Time Frame: Eight weeks
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The participant will be asked to hold a metal tipped pencil with his dominant hand for 15 seconds in the 9 holes that are gradually decreasing in size without touching the edges.
The purpose of the test will be to analyze the stability of the hand, exercise, smoking, alcohol intake, psychomotor speed, exercise and fatigue.
Errors that occur when the participant touches the hole area will be recorded digitally.
The test will be repeated 3 times on average and the result value will be calculated.
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Eight weeks
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Postural Sway Assessment
Time Frame: Eight weeks
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Postural sway was assessed using the GYKO body sway device (Microgait, Italy), a validated tool that measures sway along two axes: mediolateral and anteroposterior (Jaworski et al., 2020). During the assessment, participants were instructed to stand in an upright posture with their feet positioned 10 cm apart and to maintain this posture for a duration of 30 seconds. Each participant underwent two trials under different visual conditions: eyes open and eyes closed. The mediolateral and anteroposterior sway distances were recorded for each trial. Data were automatically captured and stored in the accompanying computer software for subsequent analysis. This protocol ensures a reliable evaluation of postural control and stability under varying sensory conditions. |
Eight weeks
|
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Upper Extremity Muscle Strength Assessment
Time Frame: Eight weeks
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MicroFET 2 muscle strength is a usable method for measuring muscle strength (Malliopoulos & Thevenon, 2002).
Muscle strength is defined as the highest (maximal) voluntary contraction that the subject can perform under specific test conditions.
The individual performed the highest voluntary contraction 3 times for each test.
The individual increases his strength for 2 seconds and maintains it at the highest level for 3 seconds.
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Eight weeks
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 3
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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