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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05574205
Other study ID # RG_20-157
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2022
Est. completion date December 1, 2023

Study information

Verified date September 2022
Source University of Birmingham
Contact Leigh Breen, PhD
Phone 121 414 4109
Email l.breen@bham.ac.uk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Dietary proteins potently augment muscle protein synthesis. Because of poorer anabolic sensitivity with ageing, studies and guidelines recommend higher dietary protein intake for older adults. Although higher doses would benefit skeletal muscle remodelling, large protein consumption is not feasible for many older adults. To circumvent, high-protein quality which possesses a high amino acid profile and digestibility appears to have an emergent role for supporting anabolism. Since currently the best line of defence against age related muscle loss is resistance exercise training and regular protein consumption, emphasising high-quality protein ingestion, such as whey protein, within meals may be feasible and efficacious in supporting musculoskeletal remodelling in older adults, without requirement for large protein doses. The investigators propose that at low doses, high quality protein will have additive benefit to muscle protein synthesis compared to low-quality protein. Further, combining high-quality protein diets with resistance exercise training will have more profound benefits for muscle protein synthesis and muscle remodelling more so than low-quality protein diets.


Description:

Participants will be randomly assigned to a 10-day dietary intervention consuming primarily animal proteins (high-quality condition) or primarily plant proteins (low-quality condition). In both conditions, participants will undertake supervised single-leg resistance exercise training every other day, amassing five days resistance exercise sessions during the study. The groups will aim to be matched and counterbalanced for gender. Equally for unilateral exercise randomisation for leg dominance will aim to be counterbalanced within both groups. Preliminary assessments: 5 days preceding the start of the dietary intervention, participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science for the following: 1. Health questionnaire 2. Written informed consent 3. Anthropometrics (Height and Weight) 4. Body fat (bioelectrical impedance) 5. Start measuring habitual activity (provided with an activity monitor and pedometer) 6. Start measuring habitual diet (provided with diet diary) 2 days preceding the start of the dietary intervention, participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science for the following: 1. Saliva sample (participant gives own saliva sample in a tube) 2. 10ml of blood taken for baseline measures (venepuncture by trained phlebotomist) 3. Loading dose of D2O (stable isotope of water ingested in 8 small 50ml doses taken 1 hour apart throughout the day) 4. Find 1 repetition maximum (1RM) during unilateral knee extension. Dietary intervention each day throughout 10-day intervention participants will provide a saliva sample and then consume a top up dose of D2O, continue wearing an activity tracker and keep a diet diary to record eating times of provided meals. Meals will be individualised to body weight for each individual to achieve a moderate protein intake of which will then consist of primarily higher quality or lower quality proteins. Day 0 (first day of diet), participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science at 0800h after fasting >10 hours the night prior for the following: 1. Resting metabolic rate (Laying down for 30 minutes to assess gaseous exchange while wearing a mask) 2. Muscle architecture (using non-invasive ultrasonography) 3. Whole-body composition assessment (DXA scan) 4. Bilateral muscle biopsies (small amount of muscle will be taken from the muscle in the thigh (vastus lateralis) by a trained person from the left and right leg, under local anaesthetic) 5. Maximal muscle strength (isometric dynamometry) and neural activation (interpolated twitch) during maximal muscle contraction on both legs in series. 6. Serial blood samples will be taken with a single cannulisation and 8 10ml blood draws taken throughout the visit (before and after consuming a breakfast which is either higher or lower in protein quality, according to the randomised condition). 7. Perceived appetite will be assessed during the visit, before and after breakfast, using visual analogue scales 8. Urine collection tub will be provided to collect urine over the next 24-hours. After consuming specified breakfast on this visit, participants will continue to eat meals given to them according to their random allocation of either higher or lower quality protein diets. Day 1, 3, 5, 7, 9 Participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science to undergo single-leg resistance exercise on a knee extension machine. Eight sets will be completed on the machine at each visit at 75% of 1RM (determined during preliminary visits and will be supervised). On day 9, the participant will be given a urine collection tub to collect urine over the next 24-hours. Day 10 (Diet finishing during this visit), participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science at 0800h after fasting >10 hours the night prior for the following assessments: 1. Resting metabolic rate (Laying down for 30 minutes to assess gaseous exchange while wearing a mask) 2. Whole-body composition assessment (DXA scan) 3. Muscle Architecture (using non-invasive ultrasonography) 4. Maximal muscle strength (Isometric Dynamometry) and neural activation during maximal muscle contraction (Interpolated twitch) 5. Bilateral muscle biopsies (small amount of muscle will be taken from the muscle in the thigh (vastus lateralis) from the left and right leg under local anaesthetic 6. Serial blood samples will be taken with a single cannulisation and 8 10ml blood draws taken throughout the visit (before and after consuming the final meal of the diet which is the breakfast which is either higher or lower in protein quality, according to the randomised condition) 7. Perceived appetite will be assessed during the visit, before and after breakfast, using visual analogue scales.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 1, 2023
Est. primary completion date October 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria: - Males and Females aged between 50-70 years - Accustomed to normal physical activity levels (averaging at least 7000 steps a day) - Healthy body mass (i.e., BMI 18-25 kg/m2) - General good health indicated by health questionnaire - Free from COVID-19 (SARS-CoV-2) symptoms. Exclusion Criteria: - Habitually high consumers of protein (>1.6g/kg/day) assessed by habitual diet diary - Food allergies - Lidocaine allergy - Smoker - Bleeding Disorders - Chronic/systemic illnesses (i.e., renal failure, rheumatoid arthritis, diabetes, poor lung function, heart disease, cancer, uncontrolled hypertension) - Regular consumption of any analgesic or anti-inflammatory drugs. Taking medications mknown to affect muscle metabolis (e.g. beta-blockers, corticosteroids).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Resistance Exercise
Supervised single-leg (unilateral) exercise will be undertaken every other day throughout the dietary intervention
Dietary Supplement:
Protein supplementation
Participants will consume a protein supplement alongside a provided diet to control protein amount and quality.

Locations

Country Name City State
United Kingdom University of Birmingham, School of Sport, Exercise and Rehabilitation Sciences Edgbaston West Midlands

Sponsors (2)

Lead Sponsor Collaborator
University of Birmingham Maastricht University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle protein synthesis using muscle biopsies and deuterated water enrichment. Muscle protein synthesis will be assessed during the high-quality and low-quality intervention and compared between exercised and controlled leg. 0-10 days
Primary Leg Strength using dynamometry Evaluating change in leg strength, of trained leg, pre- and post-intervention with high-quality and low-quality protein condition 0-10 days
Primary Neural activation using interpolated twitch Assessing change in neural activation via non-invasive interpolated twitch technique of between exercised legs pre-and post intervention in both protein quality conditions 0-10 days
Primary Muscle architecture using ultrasound Using non-invasive ultrasound to determine change of muscle structure with training between protein quality conditions. 0-10 days
Secondary Appetite regulation using questionnaires Assessing perceived hunger using a validated, 8 question, 100mm visual analogue scales. 0-10 days (3 hours postprandial)
Secondary Appetite regulation, blood Assessing the secretion of hunger and appetite hormones within the blood after meals which contain high-quality versus low-quality protein. 0-10 days (3 hours postprandial)
Secondary Metabolic rate, metabolic cart Evaluating alterations in energy expenditure before and after high-quality or low-quality protein containing meal using a metabolic cart. 0-10 days
Secondary Nitrogen balance from urine and dietary protein intake Evaluating change in nitrogen balance between adhering to high-quality or low-quality protein diets over a 10-day period 0-10 days (24-hour urine collection)
Secondary Body composition using Duel- energy x-ray absorptiometry (DXA) scan. Change in body composition (muscle mass, fat mass, bone mineral density) will be evaluated using a DXA scanner before and after adhering to single leg resistance exercise paired with either high-quality or low-quality protein diet. 0-10 days
Secondary Muscle fibre specific analysis using immunofluorescence microscopy. Evaluate changes in fibre specific differences in the distribution and localisation of key anabolic markers between trained and untrained legs for both protein quality conditions. 0-10 days
Secondary Intramuscular signalling using western blotting Evaluate changes in protein content and phosphorylation from the start to the end of the intervention. 0-10 days
Secondary Physical activity levels using accelerometery and pedometer Monitoring of habitual and habitual physical activity to evaluate if intensity and duration of activity is similar between habitual and intervention. -5-10 days
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