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Clinical Trials/NCT02714088
NCT02714088
Completed
Not Applicable

The Effect of Novel High-intensity Interval Training on Physical Fitness in Older Adults

Teesside University1 site in 1 country36 target enrollmentApril 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
High-intensity Interval Training
Sponsor
Teesside University
Enrollment
36
Locations
1
Primary Endpoint
Change in lower body muscular power
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

High-intensity interval training (HIT) has been demonstrated to be an effective strategy to improve markers of health and fitness across a wide range of healthy and clinical populations. Currently however, there is only limited evidence which has examined the effectiveness of HIT in older adults (>50 years). HIT is an appealing strategy in this group as it has the potential to impact both cardiorespiratory and muscular fitness, which both play an important role in maintaining functional fitness and quality of life in a time-efficient manner. Developing an understanding of novel strategies for delivering this type of exercise training may ultimately provide a viable alternative to traditional modes of exercise training for a broader range of participants. As such, the purpose of this study is to evaluate the effects of a novel, high-intensity interval training exercise protocol to improve physical fitness in adults aged over 50 years. This research also aims to evaluate if this type of training intervention is feasible in this population, through analysis of adherence and intervention fidelity.

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
August 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christopher Hurst

Postgraduate Researcher

Teesside University

Eligibility Criteria

Inclusion Criteria

  • Must be aged 50-85 years
  • Must be able to provide informed consent to participate
  • Must be free from all exclusion criteria

Exclusion Criteria

  • Symptoms of or known presence of heart disease of major atherosclerotic cardiovascular disease
  • Early family history of sudden cardiac death
  • Condition or injury or co-morbidity affecting the ability to undertake exercise
  • Diabetes mellitus
  • Pregnancy or likelihood of pregnancy

Outcomes

Primary Outcomes

Change in lower body muscular power

Time Frame: Baseline and following exercise training (12 weeks)

Assessed via Nottingham Leg Extensor Power Rig

Change in Aerobic fitness

Time Frame: Baseline and following exercise training (12 weeks)

Assessed via Chester step test

Change in upper extremity muscular strength

Time Frame: Baseline and following exercise training (12 weeks)

Hand grip strength assessed using handheld dynamometer

Change in quality of life

Time Frame: Baseline and following exercise training (12 weeks)

Assessed via Short form quality of life questionnaire (SF36)

Study Sites (1)

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