The Perceived Point of Muscular Discomfort vs the Point of Failure in the Ageing Population- a Pilot Study
The Perceived Point of Moderate Muscular Discomfort vs the Point of Technical Failure in the Ageing Population- a Pilot Study.
1 other identifier
interventional
15
1 country
1
Brief Summary
This is an investigation into the differences in muscle activation and numerical difference in reps between the feeling of moderate discomfort and technical failure during a set of bodyweight resistance exercise. The investigators know that resistance training is an essential tool for older people to maintain muscle function, valuable independence and autonomy in daily tasks. The idea of completing a set of resistance training activity to the point of failing a repetition due to fatigue regularly has been shown to not be appealing and could be a reason why there are low participation rates among older people for in weight training regularly. Research has also shown that it is not necessary to train to failure (being unable to continue to complete repetitions of an exercise with the proper technique due to fatigue), but the investigators would like to know if training to a point of moderate discomfort can also allow for the muscles to gain the positive changes associated with weight training, potentially making it more accessible and enjoyable. Using bodyweight exercises (a squat pattern and a push up pattern) the investigators will see how many repetitions after the point of perceived moderate discomfort is stated at which the point of failure is. the investigators will also measure muscle activation in the quadriceps and triceps with EMG (a device that can detect the muscles' electrical activity/ how hard it is working) to see at which point the muscle is working the hardest.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
February 2, 2026
CompletedStudy Start
First participant enrolled
February 10, 2026
CompletedFirst Posted
Study publicly available on registry
February 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 10, 2026
CompletedFebruary 13, 2026
February 1, 2026
28 days
February 2, 2026
February 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The number of reps between reported perceived moderate muscular discomfort and technical failure.
The quantitative difference between the rep number that the participant reports the feeling of moderate muscular discomfort at (5 on a scale of 1-10) compared to the rep number that technical failure of the set occurs.
During 1 set of body weight resistance exercise.
Secondary Outcomes (2)
Muscle Activity
During intervention
Accuracy of exercise difficulty selection
Immediately after intervention
Study Arms (1)
Bodyweight push-up and squat variations
EXPERIMENTALThe participant will select a variation of the push-up and squat. This will either be beginner, intermediate or advanced. Muscle activity in the triceps and quadriceps muscle groups will be measured for the push-up and squat patterns respectively.
Interventions
The intervention involves performing progressive variations of squat and push-up patterns to technical failure while monitored by EMG electrodes on the triceps and quadriceps. Participants verbally signal a "moderate" discomfort threshold (5/10) during each set to identify the repetition gap between perceived strain and actual physical exhaustion. This structured exercise task serves to calibrate subjective effort against objective muscle activation (%MVC) to map the physiological mechanics of fatigue.
Eligibility Criteria
You may qualify if:
- Aged 60-80 years of age.
- Physically capable of resistance training.
- Able to walk unassisted.
You may not qualify if:
- Major cardiovascular (e.g. myocardial infarction, angioplasty within the last year, coronary artery bypass graft), neurological (e.g. Parkinson's disease, Alzheimer's, major anxiety or depressive disorders), muscular (e.g., muscular dystrophies, myopathies, myositis) or uncontrolled metabolic conditions (e.g. Type 1 or 2 diabetes).
- Severe obesity (BMI \>39).
- Have undertaken regular resistance exercise in the last 12 months.
- Any upper or lower body musculoskeletal injury that impairs the participants ability to perform a repetition as fast as possible.
- Acute or terminal illnesses (e.g. severe locals or systemic infections, cancer).
- Current residence being within a setting of care.
- Experience of muscle pain from taking statins.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Lancaster University
Lancaster, Lancashire, LA1 4YW, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Paul Hendrickse, PhD
Lancaster University
- PRINCIPAL INVESTIGATOR
Lawrence Hayes, PhD
Lancaster University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD Student
Study Record Dates
First Submitted
February 2, 2026
First Posted
February 13, 2026
Study Start
February 10, 2026
Primary Completion
March 10, 2026
Study Completion
March 10, 2026
Last Updated
February 13, 2026
Record last verified: 2026-02