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Exercise and Nutrition Interventions in Age-related Sarcopenia

The Multidimensional Effects of Exercise and Nutritional Interventions on Musculoskeletal Functioning, Nutritional Status and Quality of Life in Age-related Sarcopenia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02912130
Enrollment
110
Registered
2016-09-23
Start date
2016-09-30
Completion date
2023-12-31
Last updated
2025-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscular Atrophy, Sarcopenia

Keywords

Exercise, Nutrition, Sarcopenia, Healthy Ageing, Elderly, Muscular Hypertrophy

Brief summary

This project will investigate the synergistic effects of Aerobic and Resistance type Exercise, in combination with Protein Supplementation, on; Body Composition, Musculoskeletal Functioning, Nutritional Status and Quality of Life in Age-related Sarcopenia.

Detailed description

Musculoskeletal ageing is an inevitable process associated with profound morphological and functional changes that will ultimately transition an individual from independent, to dependable living, relying heavily on personal health care for survival. The United Kingdom (UK) population aged over 65 years is expected to rise from 8.8 to 11.3 million by 2025. As life expectancy increases due to advances in medical treatment, an age-related disease termed sarcopenia, has become more prevalent in the elderly. Sarcopenia, described as the loss of musculoskeletal mass, strength and/or physical functioning with age, manifests after the 6th decade and rapidly increases after the 8th decade, resulting in a deterioration of health status and quality of life. To manage the looming health and economic consequences of sarcopenia, suitable therapeutic strategies to manage the condition are warranted. Therefore, this randomised control trial (RCT) will investigate the effects of 16-weeks of exercise and nutritional interventions in inactive senior citizens (60 - 90 years old).

Interventions

DIETARY_SUPPLEMENTProtein Supplementation

1.2-1.5g/kg/body weight per day

OTHERAerobic Exercise

30-60 minutes per week of moderate intensity exercise

OTHERResistance Exercise

60 minutes per week of progressive resistance training

Sponsors

Liverpool Hope University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Male and Female participants * 60 - 90 years of age * Resident in North West, England, UK * BMI 18.5-30 kg/m * Can speak and understand English * Willing to consent and follow the study procedures

Exclusion criteria

* Recent (i.e. past 3 months) or concurrent participation in any clinical trial or dietary and/or exercise intervention program * Self-reported lactose intolerance * Uncontrolled diabetes (HbA1C \>10) * Uncontrolled Hypertension (160/100) and uncontrolled hypotension (\<100 systolic) * Treatment with Beta Blockers, Calcium Channel Blockers, Digitalis, Bronchodilator, * Diuretics, Vasodilators * Current hormone therapy such as insulin, testosterone or hormone replacement therapy * History of falls/osteoporosis * Major psychological/mental illness * Medical conditions that precluded safe participation in an exercise program * Other major systemic diseases: Liver and kidney diseases, Advanced gastrointestinal disorders, Cardiovascular Diseases, Advanced chronic obstructive pulmonary disease, Advanced Rheumatoid Arthritis, Cancer

Design outcomes

Primary

MeasureTime frame
Body Composition: Lean Muscle/Fat Tissue 1) appendicular lean mass (kg) divided by height (meters-squared) and 2) appendicular lean mass divided by body mass index16 weeks

Secondary

MeasureTime frame
Gait speed during timed 4-meter walk (m/s)16 Weeks
Time to complete five chair rises (m/s)16 Weeks
Balance assessment: 1) feet side to side, 2) semi-tandem, 3) full tandem, and 4) single leg. Scored as Yes or No.16 Weeks
Isometric Strength - Knee Flexion/Extension: Dynanometer (Nm/Kg)16 Weeks
Muscle Fatigue: Upper & Lower limb: 25% of MVC during 60 seconds using Electromyography (EMG), measured in millivolts (mV)16 Weeks
Exercise Tolerance: Six Minute Walk Test (metres)16 Weeks
10-metre Gait analysis during habitual walking speed using Electromyography (EMG)16 Weeks
10-metre Gait analysis during habitual walking speed using Three-Dimensional Motion Capture - 1) Spatiotemporal, 2) Kinematics16 Weeks
Biochemical: Glycated Haemoglobin (HBA1c) (%)16 Weeks
Grip Strength: Hand Grip Dynanometer (kg)16 weeks
Biochemical: Insulin-Like Growth Factor 1 (IGF-1) (ng/ml)16 Weeks
Arterial Pressure: Pulse Wave Velocity (m/s)16 Weeks
Energy Balance: Periodic Food Diary (Kcal)16 Weeks
World Health Organization Quality Of Life Assessment (WHOQOL): Each question is scored from 1-5 on a response scale16 Weeks
Short-Form Health Survey (SF-12): Each question is scored between 1-6 on a response scale16 Weeks
Activities of Daily Living (ADL): Each response is scored as either: 0 or 116 Weeks
Mini-Mental State Examination (MMSE): Each correct response is scored as 1 point16 Weeks
Nutritional Status: Mini-Nutritional Assessment (MNA) - Classified as (Low, Moderate, High risk)16 weeks
Biochemical: C-Reactive Protein (CRP) (mg/L)16 Weeks

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026