The Impact of Bed Rest, Aging and NMES on Skeletal Muscle
The Impact of Bed Rest and Aging on Muscle Mass and Muscle Function: Effects of Neuromuscular Electrical Stimulation
1 other identifier
interventional
32
1 country
1
Brief Summary
Loss of muscle mass is common phenotypic trait of muscular disuse and ageing. The loss of muscle mass affects, among others, the ability to maintain homeostasis of glucose metabolism and the energy reservoir in catabolic conditions, while also affecting mechanical muscle function which can cause detrimental impairments in general functional status and hence quality of life. However, a limited amount of research has attempted to elucidate molecular regulators of muscle mass loss following bed rest in older individuals and across genders. Consequently, the mechanistic drivers are unresolved and there are currently no effective therapeutic strategies to counteract muscle wasting and loss of function in individuals submitted to bed rest e.g. during hospitalization. Purpose The purpose is to examine the effects of 5 days of bed rest on muscle mass, including myofibrillar protein synthesis and breakdown, and muscle function, and elucidate molecular regulators of muscle mass loss and metabolic pathways, while also investigating if potential negative effects can be counteracted by daily NeuroMuscular Electrical Stimulation (NMES) across different age and genders. Methods The study is designed as a randomized controlled cross-over 5-day bed rest study including a group of healthy young (18-30 years) and healthy old (65-80 years) men and women. Participants will receive daily electrical stimulation (NMES) of the thigh muscles (30 min x 3/day) on one leg (ES), while the other leg serves as a control (CON). Participants will be tested at baseline (pre) and after (post) intervention for muscle strength, muscle power, balance, and muscle activation. Blood samples are collected at several time points and muscle biopsies are sampled pre- and post-intervention along with assessment of whole-body muscle mass and thigh muscle mass. Scientific exposition The results from the study can potentially provide insight into the adaptive mechanisms associated with NMES training and muscular disuse on both cellular- and whole-body level. The understanding of the underlying mechanisms is crucial for the application of NMES in a therapeutic context and will furthermore help us understand the basic mechanism regulating the skeletal muscle mass during both training and muscular disuse. Overall, the results can potentially help establishing treatments to counteract loss of muscle mass, muscle function and muscle health during periods of muscular disuse.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 29, 2022
CompletedFirst Submitted
Initial submission to the registry
August 22, 2022
CompletedFirst Posted
Study publicly available on registry
November 15, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2024
CompletedNovember 15, 2022
November 1, 2022
10 months
August 22, 2022
November 14, 2022
Conditions
Outcome Measures
Primary Outcomes (3)
Change in Myofiber cross-sectional area
Histochemical analysis of type I and type II myofiber cross-sectional area
Change from baseline after bed rest intervention
Assessment of myofibrillar protein synthesis
Quantification of myofibrillar protein synthesis using the stable-isotope amino acid tracer deuterium oxide (D2O)
Assessed during the period from pre-intervention biopsies (day 0, first day of bed rest) to post-intervention biopsies (day 5, last day and cessation of bed rest)
Change in maximal isometric muscle strength and superimposed twitch
Maximal isometric voluntary quadriceps strength combined with the superimposed twitch technique to assess maximal strength and voluntary muscle activation
Change from baseline after bed rest intervention
Secondary Outcomes (12)
Change in total Akt protein assessed by Western blot
Change from baseline after bed rest intervention
Change in total mTOR protein assessed by Western blot
Change from baseline after bed rest intervention
Change in total MuRF-1 protein assessed by Western blot
Change from baseline after bed rest intervention
Change in total Atrogin-1 protein assessed by Western blot
Change from baseline after bed rest intervention
Change in total myostatin protein assessed by Western blot
Change from baseline after bed rest intervention
- +7 more secondary outcomes
Other Outcomes (2)
Accelerometer data
3 days prior to the intervention
Accelerometer data
Throughout the 5 day intervention
Study Arms (2)
Bed rest- Control
ACTIVE COMPARATOROne leg will be subjected to disuse by bed rest and will not receive further treatment during the bed rest period.
Bed rest + NMES
EXPERIMENTALOne leg will be subjected to disuse by bed rest and will in addition receive neuromuscular electrical stimulation of the quadriceps muscle 3 times/day.
Interventions
Unilateral neuromuscular electrical stimulation (m. Quadriceps)
Eligibility Criteria
You may qualify if:
- Healthy
- Age between 18-30 or 65-80 years
- Injury free in the lower extremities (No previous or current knee injuries or knee pain)
- Normal weight
- Consumes normal diet
You may not qualify if:
- Cognitive impairment affecting the ability to participate in the study.
- Health related contraindications to participating in the intervention (i.e., bed rest and/or NMES), such as eczema and rash on the lower extremities
- Smoker
- Obesity
- Not able to speak or understand Danish.
- Acute or chronic diseases such as diabetes, cancer, embolism, infection, cardio-vascular diseases
- Use of medication which affects myofibrillar protein synthesis or the skeletal muscle tissue
- Use of other medication (e.g. anticoagulants, adrenal cortex hormone \[within the last 3 months\] etc.)
- Previous or current use of anabolic steroids
- Previous participation in research trials involving deuterium oxide or another stable isotope tracer
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bispebjerg Hospital
Copenhagen, 2400, Denmark
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Charlotte Suetta, Professor
Bispebjerg Hospital
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The assessors will be without knowledge of which leg has received neuromuscular electrical stimulation and which leg was control
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Dr.Med
Study Record Dates
First Submitted
August 22, 2022
First Posted
November 15, 2022
Study Start
April 29, 2022
Primary Completion
February 28, 2023
Study Completion
August 1, 2024
Last Updated
November 15, 2022
Record last verified: 2022-11