Resistance Exercise Training at Different Intensities in Healthy and Frail Older People: A Feasibility Study
After the age of 40-45 years muscle mass and function progressively decline, reducing older peoples' abilities to perform tasks of daily living and also increase the risk of falls. It is known that, across the life course, resistance exercise can be of benefit in increasing muscle mass and function, yet how hard the exercise should be performed has received little attention. Current recommendations are for older people to perform exercise at 70% of the maximum they can lift, quite a high intensity that often puts older people off participating. Recent evidence in younger people has suggested that such intensities are not required.
The investigators aim to determine the feasibility of a study to investigate recruitment and adherence of older people to a study of exercise training at different intensities.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The cohort will comprise two sets of participants: frail older adults and non-frail older adults.
Each participant will receive 8 weeks of twice weekly supervised resistance training. Both the frail and non-frail participants will be randomised into either receiving high load resistance training or low load resistance training. High load resistance training will be delivered at 70% of the participants maximal capacity and low load resistance training will be delivered at 30% of maximal capacity. All resistance training will focus on the lower limb and regardless of intensity each exercise will be done to failure (unable to complete another full repetition).
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Glasgow, United Kingdom
- Recruiting
- Glasgow Royal Infirmary
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Contact:
- Evan Campbell, PhD
- Phone Number: 0141 330 3076
- Email: evan.campbell@glasgow.ac.uk
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Non-frail - Over 65 years of age Frail - Over 65 years of age, Three or more of the following criteria: >10lbs of weight loss unintentionally in previous year; grip strength in lowest 20% (by sex and BMI); self-reported exhaustion; walking time for 15 feet in slowest 20% (by sex and height); physical activity in the lowest 20%.
Exclusion Criteria:
Non-frail - Current participation in an exercise programme. Clinical team do not think resistance exercise would be safe or unable to consent. Any other reason that precludes participation in exercise, decision made by research team in consultation with a consultant in Geriatric Medicine where required.
Frail - Current participation in an exercise programme. Clinical team do not think resistance exercise would be safe or unable to consent. Any other reason that precludes participation in exercise, decision made by research team in consultation with a consultant in Geriatric Medicine where required.
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 |
|---|---|
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Active Comparator: High load non-frail
Non-frail participants who will receive resistance training at 70% of their maximal strength
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Moving muscles against loads with the purpose of increasing strength.
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Active Comparator: low load non-frail
Non-frail participants who will receive resistance training at 30% of their maximal strength
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Moving muscles against loads with the purpose of increasing strength.
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Experimental: high load frail
Frail participants who will receive resistance training at 70% of their maximal strength
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Moving muscles against loads with the purpose of increasing strength.
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Experimental: low load frail
Frail participants who will receive resistance training at 30% of their maximal strength
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Moving muscles against loads with the purpose of increasing strength.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Number of training sessions attended
Time Frame: 8 weeks
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Expressed as a percentage of number of sessions attended
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8 weeks
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Compliance with protocol
Time Frame: 8 weeks
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Expressed as a percentage of number of sessions where training protocol was adhered to
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8 weeks
|
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Number of treatment-related adverse events as assessed by CTCAE v4.0
Time Frame: 8 weeks
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Number of adverse events that could be attributed to the intervention
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8 weeks
|
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Acceptability of intervention (qualitative)
Time Frame: 8 weeks
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focus groups with semi-structured discussion plans will investigate the acceptability of the intervention
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8 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Muscle thickness
Time Frame: 8 weeks
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Thickness of vastus lateralus using ultrasound (mm)
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8 weeks
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Muscle power
Time Frame: 8 weeks
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Maximum voluntary contraction of a muscle at a set angle to produce a torque (kg)
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8 weeks
|
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Muscle strength
Time Frame: 8 weeks
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Maximal load participant can lift (kg)
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8 weeks
|
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Frailty
Time Frame: 8 weeks
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As measured by the Fried criteria.
These are low energy expenditure, slow gait speed, weak grip strength, exhaustion, and unintentional weight loss.
Fulfilling three of these criteria indicates clinical frailty.
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8 weeks
|
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Quality of life
Time Frame: 8 weeks
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Measured using the Euroqol EQ-5 Dimension- 5 Level self report measure.
This scale measures quality of life in 5 dimensions and produces an index of quality of life rangin from a worst quality of life at -1 to best quality of life at 1.
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8 weeks
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Activities of daily living
Time Frame: 8 weeks
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Measured using the Barthel index.
This scale measures ten variables of activities of daily living and produces an overall score.
This ranges from 0-20 with a higher score indicating greater independence.
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8 weeks
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Activities of daily living
Time Frame: 8 weeks
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Measured using the Lawton ADL scale.
this self report measures assess independence in daily living in 8 different domains but produces an overall score.
Scores range from 0-8 with 8 indicating full independence.
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8 weeks
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Functional abilities
Time Frame: 8 weeks
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Short performance battery test.
This battery of tests assesses balance, gait speed and lower limb strength.
Scores are awarded for each individual section and aggregated ranging from 0-12 with a higher score indicating greater physical capability.
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8 weeks
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motion analysis
Time Frame: 8 weeks
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biomechanical assessment using infr-red motion analysis cameras
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8 weeks
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Evan Campbell, PhD, Univeristy of Glasgow
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Other Study ID Numbers
- 3.0
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
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