- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06086808
Effect Of Resistance Training On Physical Fitness, Cognitive Ability, And Academic Performance In Young Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In recent years, the relationship between physical fitness, cognitive ability, and academic performance has garnered significant attention in the fields of education, psychology, and sports science. Young adulthood represents a critical developmental period characterized by substantial physical, cognitive, and psychological changes. During this phase, individuals are often engaged in academic pursuits, which makes understanding the impact of various interventions on physical fitness, cognitive ability, and academic performance especially relevant.
While individual studies have explored the effects of resistance training on physical fitness, cognitive ability, and academic performance separately, there remains a gap in the literature concerning a comprehensive understanding of their interconnectedness in the context of young adults. This study aims to bridge this gap by investigating the potential causal relationship between resistance training and these multifaceted outcomes.
This randomized controlled trial will recruit participants from young population. Study participants will be randomized into two groups: Group-A and Group-B. Group-A participants would receive resistance training for 3 consecutive months, while Group-B participants would follow general fitness and body toning exercises. Physical fitness, cognitive ability and academic performance will be measured at the baseline and after the termination of intervention program.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Noman Sadiq, MS-SPT
- Phone Number: +923145520548
- Email: noman.sadiq@riphah.edu.pk
Study Contact Backup
- Name: Tahreem Nisar, MS-SPT*
- Phone Number: +923365062152
- Email: tahreemnisar83@gmail.com
Study Locations
-
-
Islamabad Capital Territory
-
Islamabad, Islamabad Capital Territory, Pakistan, 44000
- Recruiting
- Riphah International University (RIU)
-
Contact:
- Noman Sadiq, MS-SPT
- Phone Number: +923145520548
- Email: noman.sadiq@riphah.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- School going children between the ages of 12 to 17 year
Exclusion Criteria:
- Participants with any recent musculoskeletal injury that hasn't healed.
- Any deformity or disability that could affect the participant's ability to perform physical activity.
- Any systemic disease/disorder that could affect the physical and cognitive performance of the participants.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A
Resistance Training Group
|
A resistance training program will be used as a progressive, high-intensity protocol.
The training stimulus will be provided using free weights.
The exercises will consist of bench presses, biceps curls, triceps extensions, Latissimus Dorsi pull-down exercises, hamstring curls, and calf raises.
The intensity of the training stimulus will be at a working range of 6 to 8 repetitions (2 sets).
The training stimulus will subsequently be increased using the 7-RM (repetition maximum) method when 2 sets of 6 to 8 repetitions are completed with proper form and without discomfort.
Other key strength exercises will include mini-squats, mini-lunges, and lunge walks.
The number of sets completed and the load lifted for each exercise will be recorded for each participant in every class.
|
|
Active Comparator: Group B
General Fitness and Toning Group
|
The general fitness and toning program will consist of stretching exercises, range-of-motion exercises, basic core-strengthening exercises, balance exercises, and relaxation techniques.
Key balance exercises will include tandem stand, tandem walking, and single leg stance (eyes opened and closed).
No additional loading (e.g., hand weights or resistance bands) will be applied to any of the exercises.
This group will serve to control for confounding variables such as physical training received by traveling to the training centers, social interaction, and changes in life style secondary to study participation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Isometric Strength (lbs)
Time Frame: Baseline and after end of the intervention (3 months)
|
Isometric Strength will be assessed using a Hand-held Dynamometer measuring isometric contraction force in pounds (lbs).
|
Baseline and after end of the intervention (3 months)
|
|
Endurance
Time Frame: Baseline and after end of the intervention (3 months)
|
Endurance will be assessed using the Yo Yo Intermittent Recovery Level 1 Test ranging from speed level 5 (lightest) to speed level 23 (hardest).
|
Baseline and after end of the intervention (3 months)
|
|
Agility
Time Frame: Baseline and after end of the intervention (3 months)
|
Agility will be assessed using Illinois Agility Run Test (Time to complete it in seconds).
|
Baseline and after end of the intervention (3 months)
|
|
Balance
Time Frame: Baseline and after end of the intervention (3 months)
|
Balance will be assessed using Star Excursion Balance Test (distance in each direction).
|
Baseline and after end of the intervention (3 months)
|
|
Stroop Test
Time Frame: Baseline and after end of the intervention (3 months)
|
Stroop test will be used to assess cognitive function (number of items completed during each task).
|
Baseline and after end of the intervention (3 months)
|
|
Trail Making Test
Time Frame: Baseline and after end of the intervention (3 months)
|
Trail Making Test will be used to assess cognitive function (time spent to complete the task).
|
Baseline and after end of the intervention (3 months)
|
|
Verbal Digit Span Test
Time Frame: Baseline and after end of the intervention (3 months)
|
Verbal Digit Span Test will be used to assess cognitive function (number of digits recalled correctly).
|
Baseline and after end of the intervention (3 months)
|
|
Academic Performance
Time Frame: Baseline and after end of the intervention (3 months)
|
Academic performance will be assessed using previous and subsequent school grades of the participants.
|
Baseline and after end of the intervention (3 months)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Noman Sadiq, MS-SPT, Riphah International University, Islamabad.
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
Keywords
Other Study ID Numbers
- REC/01612 Tahreem Nisar
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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