- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02714088
The Effect of Novel High-intensity Interval Training on Physical Fitness in Older Adults
October 17, 2016 updated by: Christopher Hurst, Teesside University
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
36
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Tees Valley
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Middlesbrough, Tees Valley, United Kingdom, TS1 3BA
- Teesside University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention
Participants will undertake a high-intensity interval training intervention, completing two exercise sessions per week for 12 weeks.
The exercise sessions will consist of 4 sets of 4-6 repetitions of 60s (45s high-intensity exercise, followed by 15s rest), interspersed with 3 minutes rest.
During each exercise repetition participants will be encouraged to reach >90% of their maximal heart rate.
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No Intervention: Control
Participants will not undertake any formal intervention and will be asked to maintain their usual physical activity habits and diet.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in lower body muscular power
Time Frame: Baseline and following exercise training (12 weeks)
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Assessed via Nottingham Leg Extensor Power Rig
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Baseline and following exercise training (12 weeks)
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Change in Aerobic fitness
Time Frame: Baseline and following exercise training (12 weeks)
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Assessed via Chester step test
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Baseline and following exercise training (12 weeks)
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Change in upper extremity muscular strength
Time Frame: Baseline and following exercise training (12 weeks)
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Hand grip strength assessed using handheld dynamometer
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Baseline and following exercise training (12 weeks)
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Change in quality of life
Time Frame: Baseline and following exercise training (12 weeks)
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Assessed via Short form quality of life questionnaire (SF36)
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Baseline and following exercise training (12 weeks)
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Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Heart rate during high-intensity interval training exercise sessions
Time Frame: Up to 12 weeks
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Up to 12 weeks
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Rating of perceived exertion (RPE) during high-intensity interval training exercise sessions
Time Frame: Up to 12 weeks
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Up to 12 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2016
Primary Completion (Actual)
August 1, 2016
Study Registration Dates
First Submitted
March 8, 2016
First Submitted That Met QC Criteria
March 15, 2016
First Posted (Estimate)
March 21, 2016
Study Record Updates
Last Update Posted (Estimate)
October 18, 2016
Last Update Submitted That Met QC Criteria
October 17, 2016
Last Verified
October 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- TEES-CH170216-SSSBL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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