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The goal of this interventional study is to learn about the role of mitochondrial function in healthy aging, and then go on and assess the role of a home-based exercise program on the changes seen. The main question[s] it aims to answer are:
The older participants will be invited to take part in a home-based 4 week exercise intervention involving either:
Full description
The study will aim to recruit 40 healthy male and female volunteers. They will be assigned into one of three groups;
All volunteers will undergo a full consenting process and undergo a full screening to ensure eligibility prior to commencing the study. If eligible for inclusion in the study, the time commitment will vary from a single half-day study visit, to 12 training sessions over a 4-week period (3 sessions per week) and two half-day study visits (one before and one after the training sessions) depending on the participant's age.
All participants will attend fasted from 22:00 the previous day. Participants will first have a single muscle biopsy of the vastus lateralis before a dual-energy x-ray absorptiometry (DXA) scan to assess body composition and an ultrasound scan of the thigh to assess the muscle structure. A supervised cardiopulmonary exercise testing (CPET) to determine cardiorespiratory fitness will then be performed before a battery of physical function assessments to determine muscle and neuromuscular function. The biopsies will be assessed using an OROBOROS respirometer for the primary endpoint of mitochondrial activity, as well being used to determine cell signaling activity and gene expression.
For those under 65 years of age, a follow-up visit 4-6 days after the biopsy for stitch removal and to complete an end of study questionnaire would be the end of the study. Those volunteers over the age of 65 years will be randomly allocated to a RET group or HIIT group for a 4-week period, after which the assessments from the baseline study day would be repeated. Each exercise group will contain 8 participants (4 male, 4 female).
Training program:
All exercise training will take place within the volunteers own homes in accordance to the divisional policy on this. As well as the education session provided at the baseline study day, participants will be contacted weekly via telephone or video call to encourage participation, to answer any difficulties participants maybe experiencing and to ensure no adverse symptoms are being experienced. A video will be recorded of a member of the research team performing the exercise regimen to enable participants to watch from home.
Each HIIT session last 15 minutes. Participants will be asked to measure their own heart rate during their rest periods and provided with an estimated max heart rate which they should be aiming to achieve within the final 2 exercises. Participants will be provided with a logbook to record the heart rate achieved in each exercise. The regimen will include:
2 min warm-up: jogging on the spot
Each of the following exercises performed for 60seconds, interspaced by 90 seconds rest
2 min cool-down: jogging on the spot
Each HIIT session lasts an estimated 20minutes. Participants will be provided with a set of TheraBand resistance bands to provide resistance to their workout, and a logbook to record the number of repetitions and band used.
Each session will include:
Each exercise will be separated by 1-minute rest, with participants encouraged to workout to mild fatigue on their final repetition in each set. If able to perform more than the allocated maximum of 15 repetitions prior to fatigue, then participants will be informed to increase the resistance by using a tougher TheraBand.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
● Current participation in a formal exercise regime
Inability to use a static exercise bike
A BMI <18 or >35 kg/m2
Active cardiovascular disease:
Taking beta-adrenergic blocking agents
Cerebrovascular disease:
Respiratory disease including:
Malignancy
Clotting dysfunction
Significant musculoskeletal or neurological disorders
Any suspected or confirmed diagnosis of Covid-19
Primary purpose
Allocation
Interventional model
Masking
32 participants in 2 patient groups
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Central trial contact
Thomas FF Smart; Bethan Phillips
Data sourced from clinicaltrials.gov
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