Effect Of Resistance Training On Physical Fitness, Cognitive Ability, And Academic Performance In Young Adults

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06086808
Collaborator
(none)
20
1
2
5.6
3.6

Study Details

Study Description

Brief Summary

The goal of this study is to determine the effect of resistance training on physical fitness, cognitive ability, and academic performance in young adults. This would be a randomized controlled trail in which participants will be randomly allocated in to two groups. One group will perform resistance training and other group will perform balance and general body toning exercises.

Condition or Disease Intervention/Treatment Phase
  • Other: Resistance Training
  • Other: General Fitness and Toning
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Concurrent Parallel Randomized Clinical TrialConcurrent Parallel Randomized Clinical Trial
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect Of Resistance Training On Physical Fitness, Cognitive Ability, And Academic Performance In Young Adults
Actual Study Start Date :
Aug 15, 2023
Anticipated Primary Completion Date :
Nov 30, 2023
Anticipated Study Completion Date :
Jan 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A

Resistance Training Group

Other: Resistance Training
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

Other: General Fitness and Toning
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.

Outcome Measures

Primary Outcome Measures

  1. Isometric Strength (lbs) [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).

  2. Endurance [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).

  3. Agility [Baseline and after end of the intervention (3 months)]

    Agility will be assessed using Illinois Agility Run Test (Time to complete it in seconds).

  4. Balance [Baseline and after end of the intervention (3 months)]

    Balance will be assessed using Star Excursion Balance Test (distance in each direction).

  5. Stroop Test [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).

  6. Trail Making Test [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).

  7. Verbal Digit Span Test [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).

  8. Academic Performance [Baseline and after end of the intervention (3 months)]

    Academic performance will be assessed using previous and subsequent school grades of the participants.

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Riphah International University (RIU) Islamabad Islamabad Capital Territory Pakistan 44000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Noman Sadiq, MS-SPT, Riphah International University, Islamabad.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT06086808
Other Study ID Numbers:
  • REC/01612 Tahreem Nisar
First Posted:
Oct 17, 2023
Last Update Posted:
Oct 17, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University

Study Results

No Results Posted as of Oct 17, 2023