Adaptive Response of Brain Towards Resistance Training in Healthy Individuals
1 other identifier
interventional
100
1 country
1
Brief Summary
The novelty of this study is to identify the mechanism of nervous system by applying resistance training intervention in healthy individuals.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 18, 2023
CompletedFirst Submitted
Initial submission to the registry
October 31, 2023
CompletedFirst Posted
Study publicly available on registry
May 14, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 29, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedMay 14, 2024
May 1, 2024
1.4 years
October 31, 2023
May 9, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
NCS (Motor Nerve Conduction Study)
To determine how fast or slow the nerves are conducting an electrical current using F wave
• 0 week • 8th week
EEG (Electroencephalography)
To measure the electrical activity of the brain using alpha and beta waves
• 0 week • 8th week
Dynamometer
To measure the strength after resistance training
• 0 week • 4th week • 8th week
Estimation of Albumin & Globulin ratio
To measure the total amount of protein in blood and effects of resistance training
• 0 week • 8th week
Study Arms (2)
Hyper Training Group
EXPERIMENTAL2 training session per week for 2 months, 1 set of 10 unloaded repetitions in arms as a warm-up, 4 sets with a goal of 8-12 repetitions with 90 seconds of rest between sets and elbows had to be fully locked out to be counted as a repetition, 1.5 seconds for concentric and 1.5 seconds for eccentric portion.
1 Repetition Maximum Group
ACTIVE COMPARATOR2 training session per week for 2 months, 1 set of 10 unloaded repetitions in arms as a warm-up, training protocol consisted of 5 attempts to lift as much weight as possible one time for that training visit with 90 seconds of rest between attempts. The load was progressively increased each attempt to try to reach or exceed their previous 1RM.
Interventions
Experimental group will perform 2 training session per week for 2 months, 1 set of 10 unloaded repetitions in arms as a warm-up, 4 sets with a goal of 8-12 Reps with 90 seconds rest between sets. 1.5 second concentric and 1.5 second eccentric contraction of bench press, The elbows had to be fully locked out to be counted as a repetition.
2 training session per week for 8 weeks, 1 set of 10 unloaded repetitions in arms as a warm-up, 1 Repetition maximum training group consisted of 5 attempts to lift as much weight as possible one time for that training visit with 90 seconds of rest between attempts, the load was progressively increased each attempt to try to reach or exceed their previous 1 repetition maximum.
Eligibility Criteria
You may qualify if:
- Body Mass Index should be 18.5-24.9 kg/m2.
- Participants were untrained and had not engaged in resistance exercise within 6 months prior to beginning the study.
You may not qualify if:
- Participants with any kind of Gastrointestinal Tract disturbance will be excluded from the study.
- Participants with any kind of Musculoskeletal injury will be excluded from the study.
- Participant with any kind of Neurological disturbance will be excluded from the study.
- Participants who use tobacco products within the previous 6 months.
- Participants who take any type of medication within the previous 6 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
PSRD Hospital
Lahore, Punjab Province, 54000, Pakistan
Related Publications (22)
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PMID: 26499819BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
Danish Latif, PhD*
PSRD College of Rehabilitation Sciences
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 31, 2023
First Posted
May 14, 2024
Study Start
August 18, 2023
Primary Completion
December 29, 2024
Study Completion
December 31, 2024
Last Updated
May 14, 2024
Record last verified: 2024-05
Data Sharing
- IPD Sharing
- Will not share