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Preventing Bed-rest Induced Muscle Loss in the Elderly

Primary Purpose

Muscle Loss, Disuse Atrophy, Protein Metabolism

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Resistance exercise
Sponsored by
University of Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Muscle Loss

Eligibility Criteria

65 Years - 80 Years (Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Males aged between 65-80 years
  • No history of structured resistance training within 10 years prior to study participation.
  • Generally good health as indicated by a thorough health questionnaire.
  • A score of ≥9 points on the Short Physical Performance Battery to assess lower extremity function.
  • Body Mass Index <30kg/m2

Exclusion Criteria:

  • Coagulation disorders
  • Myocardial infarction
  • Artery/vein disease
  • Hormone replacement therapy
  • Other chronic/systemic illnesses (i.e. renal failure, chronic obstructive pulmonary disease, cancer).
  • Undergone 2 or more muscle biopsies from each leg previously.
  • Received a stable isotope infusion in the last 3 years prior to study enrollment.

Sites / Locations

  • University of Birmingham, School of Sport, Exercise and Rehabilitation Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Single Exercise

Multi Exercise

Arm Description

Subjects allocated to this group will perform a single bout of one-legged resistance exercise. This bout will take place 1 day prior to the start of the bed rest. The resistance exercise will consist of 8 sets of leg extensions and 8 sets of leg curls. The non-exercising leg will serve as an internal control. The dominant leg will perform the exercise.

Subjects allocated to this group will perform 4 bouts of one-legged resistance exercise. These bouts will take place on alternate days the week leading up to the bed rest. Each resistance exercise bout will consist of 8 sets of leg extensions and 8 sets of leg curls. The non-exercising leg will serve as an internal control. The dominant leg will perform the exercise.

Outcomes

Primary Outcome Measures

Integrated myofibrillar protein synthesis rates
Myofibrillar protein synthesis rates will be measured during the prehabilitation and bed rest period in both the exercising and resting leg.
Muscle mass via MRI
Muscle volume in the quadriceps will be assessed before and after bed rest using magnetic resonance imaging techniques

Secondary Outcome Measures

Muscle fibre properties
Via immunohistochemical staining procedures muscle fibre cross sectional area will be determined
Physical activity levels
Daily average time spent in sedentary, light, moderate or vigorous intensity activity using an accelerometer
Step-count
activity will be determined using accelerometry. Furthermore, step count will be Daily step-count assessed using a hip-worn pedometer
Plasma biomarkers of metabolic health
Blood markers - serum total cholesterol, serum high-density lipoprotein cholesterol, serum non-high-density lipoprotein cholesterol, total cholesterol, serum non-esterified fatty acids, serum triglycerides (units of measure for all - mmol/L)
Serum insulin
Via ELISA kits, resting insulin will be assessed using baseline plasma samples from before and after the bed rest period (pmol/l)
Intramuscular signaling via western blot
Western blots for phosphorylation of key anabolic and catabolic signaling proteins will be performed.
Gene expression
Search Results Web results Reverse transcription polymerase chain reaction (RT-PCR) will be performed to assess gene-expression of muscle anabolic and catabolic genes.
Dietary intake
Dietary intake will be assessed using 3-day weighed food diaries.
Body composition
Bioelectrical impedance analysis will be used to determine whole body fat and fat-free mass (units are % of total body mass for both fat and fat-free mass).
Leg strength
Estimated maximal leg strength will be determined for the leg extension and leg curl before and after the bed rest period
Height
measured using a stadiometer (cm)
Body weight
Measured using a digital weighing scale (kg)
Body Mass Index
Weight and height will be combined to report BMI in kg/m^2

Full Information

First Posted
June 1, 2020
Last Updated
June 4, 2020
Sponsor
University of Birmingham
Collaborators
Biotechnology and Biological Sciences Research Council, University of Nottingham
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1. Study Identification

Unique Protocol Identification Number
NCT04422665
Brief Title
Preventing Bed-rest Induced Muscle Loss in the Elderly
Official Title
Exercise 'Prehabilitation': A Novel Intervention to Protect Against Disuse-induced Muscle Atrophy and Sarcopenia in the Old
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
September 1, 2017 (Actual)
Primary Completion Date
October 1, 2019 (Actual)
Study Completion Date
January 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Birmingham
Collaborators
Biotechnology and Biological Sciences Research Council, University of Nottingham

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Episodes of inactivity due to hospitalisation, as short as 5 days, are associated with rapid muscle and strength loss in the elderly. The observed muscle loss with inactivity is likely due to muscle anabolic resistance and increased breakdown rates of muscle tissue. This is of great concern as the average hospital stay in the elderly is 5-6 days. Moreover, minor illnesses not requiring hospitalisation generally require short-term periods of inactive home-based recovery. The accumulation of repeated disuse events in older individuals manifests in a chronic muscle anabolic resistance (i.e. the inability of muscle to respond to anabolic stimuli such as exercise and nutrition) that may underpin the slow but devastating process of age-related muscle loss. It is our belief that strategies to promote muscle health in ageing and reduce healthcare expenditure, should focus on alleviating muscle deterioration and anabolic resistance during short-term disuse. In this regard, we propose that resistance exercise (i.e. weight lifting) performed prior to a disuse event (termed 'prehabilitation') may be sufficient to offset muscle loss in older individuals. Thus, we suggest the potent effect of resistance exercise in older muscles may prevent muscle loss during short-term disuse.
Detailed Description
Participants will be assigned to either single-bout (SINGLE; n=10) or multiple-bouts (MULTI; n=10) of resistance exercise prehabilitation prior to 5 consecutive days of bed rest. Groups will be matched for age, anthropometric characteristics and activity levels. Only males will be studied due to potential gender differences in muscle protein turnover. A single-leg resistance exercise prehabilitation model will allow for a direct within-subject comparison against the non-exercised control leg. Preliminary Assessments Following an induction meeting and obtainment of informed consent, participants will report to The National Institute of Health/Wellcome Trust Clinical Research Facility (CRF) at University Hospital Birmingham (UHB) at 0800h having fasted from 2100h the previous night. After measuring height and weight, the following parameters will be determined in the order outlined: Muscle biopsy, blood and saliva sampling: a muscle biopsy sample will be obtained from a specific thigh muscle under local anaesthetic. A blood sample will then be obtained from a forearm vein. Participants will also provide a saliva sample. This will be obtained prior to the following measurements. Lower-limb function: The short physical performance battery (SPPB) test will be used. Body composition: bioelectrical impedance analysis will be used to determine fat/fat-free mass on a whole-body and anatomical regional basis (CRF nurse). Muscle size/architecture: The thickness of the thigh muscles will be determined via non-invasive ultrasound imaging. Leg strength and muscle activation: Estimated maximal leg strength will be measured firstly on a standard knee extension exercise machine. Stable isotope procedure: Immediately following muscle biopsy, blood and saliva sampling, participants will orally consume a small bolus of 'heavy water' tracer to label the body water pool with a small amount of this isotope. Participants will provide a daily saliva sample to monitor body water tracer enrichment. This technique will allow us to quantify muscle protein synthesis over the course of prehabilitation and bed-rest. Participants will be fitted with an accelerometer and pedometer to asses daily activity levels. Participants are given a food diary to record daily nutritional intake over a 3-day period. Exercise Prehabilitation (Days 0-7) Participants will be randomly assigned to undergo 4 resistance exercise bouts the week before (Day 1, 2, 5 and 7), or 1 resistance exercise bout on the evening prior to bed rest (i.e. Day 7). Exercise bouts will consist of 8 sets of single-leg knee extension exercise and 8 sets of single-leg leg curls. The non-exercised control leg will remain passive throughout training. Resistance exercise will be performed at 70% of previously determined maximal strength (10-15 repetitions). Intervention - 5-days of bed-rest (Days 8-13) Participants will report to the CRF at 0700h the morning immediately after exercise prehabilitation phase. At 0800h, muscle biopsies will be obtained from both legs to assess changes in muscle metabolism over the 7 days of prehabilitation. Participants will then be transported for dual energy x-ray absorptiometry (DXA), Magnetic Resonance Imaging (MRI) and ultrasound assessment of body/muscle composition, after which the 5 consecutive days of strict bed rest will begin. The bed rest model will mimic a traditional inpatient hospital stay and reflect the level of muscle unloading that occurs in older individuals following acute illness. Participants will spend the majority of time in bed and will be allowed to adjust the hospital bed head height for reading, eating and watching television, but will otherwise be instructed to lie flat in bed. Bathing/hygiene will be performed in a wheelchair at a sink. The bathroom accessed using a wheelchair. Adherence to bed rest will be monitored by nursing staff and through daily analysis of accelerometry data. Post Intervention Assessments (Day 13) On the morning after completion of the 5-day bed rest phase (i.e. Day 13) participants will awake at 0700h in the CRF and remain in bed for assessment of muscle protein synthesis in trained and untrained control legs. A cannula will be inserted into a vein of both forearms for frequent blood sampling and a stable isotope tracer infusion. During the tracer infusion, muscle biopsies will be obtained from both trained and untrained legs before and after consumption of a milk protein drink, to assess muscle metabolism. Participants will then be transported by wheelchair for repeat bioelectrical impedance analysis, MRI and ultrasound scans to assess body/muscle composition. Leg strength will be reassessed in trained and untrained legs. A physiotherapist will perform a functional assessment of participants before they are discharged. Rehabilitation Training Participants will be given the opportunity to complete a 6-week rehabilitation programme, consisting of a progressive 3 x weekly leg resistance training with protein supplementation, designed to fully restore any loss in muscle mass and strength from short-term bed rest. Resistance training rehabilitation will not form a specific study objective, but muscle size and strength will be assessed to ensure restoration of any muscle decline from bed rest.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Loss, Disuse Atrophy, Protein Metabolism, Prehabilitation, Sarcopenia

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly allocated to one of two intervention groups. Due to the single-legged typed of resistance exercise, each subject will be its own control.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single Exercise
Arm Type
Experimental
Arm Description
Subjects allocated to this group will perform a single bout of one-legged resistance exercise. This bout will take place 1 day prior to the start of the bed rest. The resistance exercise will consist of 8 sets of leg extensions and 8 sets of leg curls. The non-exercising leg will serve as an internal control. The dominant leg will perform the exercise.
Arm Title
Multi Exercise
Arm Type
Experimental
Arm Description
Subjects allocated to this group will perform 4 bouts of one-legged resistance exercise. These bouts will take place on alternate days the week leading up to the bed rest. Each resistance exercise bout will consist of 8 sets of leg extensions and 8 sets of leg curls. The non-exercising leg will serve as an internal control. The dominant leg will perform the exercise.
Intervention Type
Other
Intervention Name(s)
Resistance exercise
Intervention Description
Single-legged resistance exercise
Primary Outcome Measure Information:
Title
Integrated myofibrillar protein synthesis rates
Description
Myofibrillar protein synthesis rates will be measured during the prehabilitation and bed rest period in both the exercising and resting leg.
Time Frame
2 years
Title
Muscle mass via MRI
Description
Muscle volume in the quadriceps will be assessed before and after bed rest using magnetic resonance imaging techniques
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Muscle fibre properties
Description
Via immunohistochemical staining procedures muscle fibre cross sectional area will be determined
Time Frame
2 years
Title
Physical activity levels
Description
Daily average time spent in sedentary, light, moderate or vigorous intensity activity using an accelerometer
Time Frame
2 years
Title
Step-count
Description
activity will be determined using accelerometry. Furthermore, step count will be Daily step-count assessed using a hip-worn pedometer
Time Frame
2 years
Title
Plasma biomarkers of metabolic health
Description
Blood markers - serum total cholesterol, serum high-density lipoprotein cholesterol, serum non-high-density lipoprotein cholesterol, total cholesterol, serum non-esterified fatty acids, serum triglycerides (units of measure for all - mmol/L)
Time Frame
2 years
Title
Serum insulin
Description
Via ELISA kits, resting insulin will be assessed using baseline plasma samples from before and after the bed rest period (pmol/l)
Time Frame
2 years
Title
Intramuscular signaling via western blot
Description
Western blots for phosphorylation of key anabolic and catabolic signaling proteins will be performed.
Time Frame
2 years
Title
Gene expression
Description
Search Results Web results Reverse transcription polymerase chain reaction (RT-PCR) will be performed to assess gene-expression of muscle anabolic and catabolic genes.
Time Frame
2 years
Title
Dietary intake
Description
Dietary intake will be assessed using 3-day weighed food diaries.
Time Frame
2 years
Title
Body composition
Description
Bioelectrical impedance analysis will be used to determine whole body fat and fat-free mass (units are % of total body mass for both fat and fat-free mass).
Time Frame
2 years
Title
Leg strength
Description
Estimated maximal leg strength will be determined for the leg extension and leg curl before and after the bed rest period
Time Frame
2 years
Title
Height
Description
measured using a stadiometer (cm)
Time Frame
2 years
Title
Body weight
Description
Measured using a digital weighing scale (kg)
Time Frame
2 years
Title
Body Mass Index
Description
Weight and height will be combined to report BMI in kg/m^2
Time Frame
2 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Males aged between 65-80 years No history of structured resistance training within 10 years prior to study participation. Generally good health as indicated by a thorough health questionnaire. A score of ≥9 points on the Short Physical Performance Battery to assess lower extremity function. Body Mass Index <30kg/m2 Exclusion Criteria: Coagulation disorders Myocardial infarction Artery/vein disease Hormone replacement therapy Other chronic/systemic illnesses (i.e. renal failure, chronic obstructive pulmonary disease, cancer). Undergone 2 or more muscle biopsies from each leg previously. Received a stable isotope infusion in the last 3 years prior to study enrollment.
Facility Information:
Facility Name
University of Birmingham, School of Sport, Exercise and Rehabilitation Sciences
City
Edgbaston
State/Province
West Midlands
ZIP/Postal Code
B15 2TT
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

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Preventing Bed-rest Induced Muscle Loss in the Elderly

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