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Clinical Trials/NCT03627793
NCT03627793
Unknown
N/A

Resistance Exercise Training at Different Intensities in Healthy and Frail Older People: A Feasibility Study

University of Glasgow1 site in 1 country60 target enrollmentAugust 21, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Frail Elderly Syndrome
Sponsor
University of Glasgow
Enrollment
60
Locations
1
Primary Endpoint
Number of training sessions attended
Last Updated
7 years ago

Overview

Brief Summary

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.

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).

Registry
clinicaltrials.gov
Start Date
August 21, 2018
End Date
November 29, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr Evan Campbell

Research Associate

University of Glasgow

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Number of training sessions attended

Time Frame: 8 weeks

Expressed as a percentage of number of sessions attended

Compliance with protocol

Time Frame: 8 weeks

Expressed as a percentage of number of sessions where training protocol was adhered to

Number of treatment-related adverse events as assessed by CTCAE v4.0

Time Frame: 8 weeks

Number of adverse events that could be attributed to the intervention

Acceptability of intervention (qualitative)

Time Frame: 8 weeks

focus groups with semi-structured discussion plans will investigate the acceptability of the intervention

Secondary Outcomes

  • Muscle strength(8 weeks)
  • Muscle power(8 weeks)
  • Muscle thickness(8 weeks)
  • Frailty(8 weeks)
  • Quality of life(8 weeks)
  • Activities of daily living(8 weeks)
  • Functional abilities(8 weeks)
  • motion analysis(8 weeks)

Study Sites (1)

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