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Ageing WellLHMA PilotNCT07473297

A Pilot Study on Skeletal Muscle Proteome Dynamics in Younger and Older Men Undertaking Normal Activity or Resistance Exercise Training.

A study testing Resistance Exercise in people with Ageing Well, run by Liverpool John Moores University at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this basic research study is to investigate effect of resistance exercise on the quality of muscle proteins in younger and older men. The main question[s] it aims to answer [is/are]: whether there is a difference in muscle protein quality between younger and older adults and if resistance exercise training… Read more about this study

Who is it for?
Ages 20 to 75 years, men onlyHealthy volunteers can take part
Conditions the study is for
Ageing Well
What is being tested?
Resistance Exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
8 participants
Where
1 siteUnited Kingdom
Study dates
10 Mar 2023to 28 Aug 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 75 years
  • Men only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Male
  • Age 25-35 OR 65-75 years

Who cannot join

  • female
  • take part in >3 bouts of endurance/resistance based training per week
  • are pregnant
  • have any previous diagnosis of ischaemic heart disease, diabetes mellitus myopathy or any neuromuscular disorder.
  • take any anticoagulant medications such as warfarin
  • have a current musculoskeletal injury.
Show all 10Show fewer
  • currently unwell with cold or flu
  • have a chronic connective tissue disorder
  • have a cardiovascular disease
  • are currently enrolled in any other research study

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Liverpool John Moores University

    Liverpool, Merseyside, L3 3AF

Other trials in United Kingdom

About this study

Official title: Proteome Dynamics to Inform Healthy Muscle Ageing

The goal of this basic research study is to investigate effect of resistance exercise on the quality of muscle proteins in younger and older men. The main question[s] it aims to answer [is/are]: whether there is a difference in muscle protein quality between younger and older adults and if resistance exercise training has a beneficial impact on the quality of muscle proteins? Participants will perform five bouts of unilateral leg press exercise during a 14 day period of deuterium oxide consumption and biopsy samples will be taken from both their exercised leg and non-exercised leg before and after the intervention period to enable the measurement of muscle protein abundances and turnover rates.

Read the detailed description

Experimental Intervention Baseline muscle biopsy On day -1 of the experimental intervention (around 7 days after the initial assessment), you will need to arrive at the laboratory at ~8 am after an overnight fast. A blood sample (7 ml) will be collected via venipuncture and muscle samples will be collected by percutaneous biopsy of the vastus lateralis (quadriceps) of each leg (see below for more detail).

Deuterium Oxide consumption On the next day (Experiment Day 0) you will consume the stable isotope, deuterium oxide (D2O - see below for more details), which is a tracer that can be used to measure the turnover rate of proteins inside you muscle. You will consume a dose of 13.3 ml D2O per kg body weight on Day 0. This equates to ~1 L of liquid for a person of 75 kg body weight. The liquid must be consumed in 4 doses of ~250 ml each at 2 h intervals, during which time you will be monitored for potential side effect (see below) by the research team, this means you will need to be available for 6 h on this day. (N.B. during this period you will have access to office and catering facilities on the LJMU Byrom Street site). On subsequent days of the experiment you will need to consume one maintenance dose of 0.67 ml D2O per Kg body weight (e.g. 50 ml for a person of 75 kg body weight) - self-administered each day, at a standardised time of day until day 14.

Unilateral leg-press exercise On days 1, 4, 7, 10 and 13 of the experimental intervention, you will perform supervised single-legged resistance exercise (unilateral leg-press) at a standardised time of day. Each session will begin with a warm-up consisting of 5 repetitions at 70 % of 10RM. You will then perform three sets of 10 repetitions at a lifting intensity of 90 % of 10 RM with 2- to 3-min rest between sets. On days 1 and 7 we will collect a venous blood sample (7 ml) and a finger-prick blood sample (~0.2 ml).

Post-intervention muscle biopsy On day 15 of the experimental intervention, you will arrive at the laboratory at 8 am after an overnight fast. A blood sample (7 ml) will be collected via venipuncture and muscle samples will be collected by percutaneous biopsy of the vastus lateralis (quadriceps) of each leg.

Post-intervention muscle function test On day 18 of the experimental intervention, isokinetic torque of the knee extensor muscles will be assessed via isokinetic dynamometry (IKD). Consistent with the initial assessment (Experiment day -7), you will first perform a warm-up (5 min at 50 W on a cycle ergometer) and then complete a test protocol consisting of four consecutive maximal knee extension movements of each leg at two different fixed movement velocities, 1.05 rad.sec-1 (60 deg.sec-1) and 3.14 rad·sec-1 (180 deg.sec-1) from which peak torque (Nm) data will be recorded. This assessment will be scheduled at a time of day roughly equivalent to that of your initial visit.

Conditions
Ageing Well
Being tested
Resistance Exercise
Keywords
Liverpool Healthy Muscle Ageing Pilot

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Resistance ExerciseOther

    Unilateral leg press. Participants undertook a supervised training session of unilateral leg-press exercise at a standardized time of day. During each session, participants performed a warm-up consisting of 5 repetitions at 70 % of 10RM. Participants performed three sets of 10 repetitions at a lifting intensity of 90 % of 10 RM with 2- to 3-min rest between sets.

Study groups in NCT07473297
Study groupRoleWhat they receive
Unilateral resistance exercise trainingOtherUnilateral resistance exercise of the dominant leg using leg press exercise
Receives: Other: Resistance Exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Muscle proteome dynamics

    Assessment of muscle proteome quality using dynamic proteome profiling to measure the abundances and turnover rates of muscle proteins.

    Measured: Throughout the 14 day intervention period of unilateral leg press exercise.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Mar 2026
  2. Study start10 Mar 2023
  3. Primary completion12 Mar 2023
  4. Study completion28 Aug 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Model description
Unilateral resistance exercise training
Masking
None (open label)
Enrolment
8 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07473297
Sponsor's protocol ID
22/SPS/075
Acronym
LHMA Pilot
Status last verified
Mar 2026
First submitted
3 Mar 2026
Last updated
16 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Only anonymised data will be generated

Questions about this trial

What is this clinical trial studying?

A study testing Resistance Exercise in people with Ageing Well, run by Liverpool John Moores University at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Muscle proteome dynamics (time frame: Throughout the 14 day intervention period of unilateral leg press exercise.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Mar 2026.

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LHMA Pilot Clinical Trial NCT07473297 | AzTrials