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Influence of Sedentary Time on Skeletal Muscle Protein Metabolism

Influence of Increased Sedentary Time on Long-term Rates of Skeletal Muscle Protein Synthesis in Young Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02624011
Enrollment
8
Registered
2015-12-08
Start date
2016-03-31
Completion date
2018-02-28
Last updated
2018-10-11

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

Conditions

Sedentary Lifestyle

Brief summary

This study will investigate the influence of increased sedentary time on long-term measures of muscle protein synthesis and metabolic health. The investigators will test the hypothesis that increased time spent in sedentary behaviours will lead to a reduction in long-term measures of muscle protein synthesis and compromised metabolic health.

Detailed description

Sarcopenia, the loss of muscle mass with age, is thought to be accelerated by an inactive, sedentary lifestyle. Increased sedentary time has consistently been associated with lower muscle mass and compromised metabolic health. However, there is currently a lack of direct evidence to support these associations. Therefore, this study will investigate whether increased sedentary time (reduced step count and exercise cessation) directly influences long-term measures of muscle protein synthesis and metabolic health in young, active adults. Following a 7 day period of normal habitual physical activity, participants will undertake a 7 day period of step reduction and exercise cessation. It is hypothesised that 7 days of increased sedentary time will result in a reduction in long-term rates of muscle protein synthesis and a worsening of metabolic health.

Interventions

BEHAVIORAL7 days of habitual physical activity followed by 7 days of reduced physical activity

Young, active participants will undergo a 7 day period of habitual physical activity followed by a 7 day period of step reduction and exercise cessation.

Sponsors

Maastricht University
CollaboratorOTHER
University of Birmingham
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Body mass index (18.5-29.99 kg/m2) * Active - defined as: ≥ 7000 steps per day (assessed during screening) and taking part in regular exercise (defined as participation in ≥ 3 sessions of aerobic and/or resistance exercise type sessions a week for ≥ 6 months prior to recruitment) * Good general health

Exclusion criteria

* Lidocaine allergy * Hypertension (≥140/90 mmHg) * Current participation in another clinical study * Previous participation in this study * Bleeding disorder/s * Current or recent smoker * Past history of substance abuse and/or taking prescription or non-prescription medication (e.g., beta-blockers, insulin or thyroxine) or supplements that may influence normal metabolic responses. * Participants who have previously (within 5 years of the present study) had 4 or more muscle biopsies obtained from the thigh quadriceps region will be ineligible.

Design outcomes

Primary

MeasureTime frameDescription
Muscle protein synthesis (FSR %/day)0-14 daysLong-term muscle protein synthesis (FSR %/day) will be determined using deuterium oxide (D2O) to compare muscle protein synthesis rates over the first 7 day period and the second 7 day period.

Secondary

MeasureTime frameDescription
Rate of fat oxidation during an oral glucose tolerance test (g/min)At 0, 30, 60, 90 and 120min of the oral glucose tolerance test at day 7 and day 14Whole body oxygen consumption (VO2, L/min) and carbon dioxide production (VCO2, L/min) following an oral glucose drink will be measured using indirect calorimetry to calculate the rate of fat oxidation during an oral glucose tolerance test (g/min).
Rate of carbohydrate oxidation at rest (g/min)For 20 minutes at day 7 and day 14Whole body oxygen consumption (VO2, L/min) and carbon dioxide production (VCO2, L/min) at rest will be measured using indirect calorimetry to calculate the rate of carbohydrate oxidation at rest (g/min).
Rate of carbohydrate oxidation during an oral glucose tolerance test (g/min)At 0, 30, 60, 90 and 120min of the oral glucose tolerance test at day 7 and day 14Whole body oxygen consumption (VO2, L/min) and carbon dioxide production (VCO2, L/min) following an oral glucose drink will be measured using indirect calorimetry to calculate the rate of carbohydrate oxidation during an oral glucose tolerance test (g/min).
Rate of fat oxidation at rest (g/min)For 20 minutes at day 7 and day 14Whole body oxygen consumption (VO2, L/min) and carbon dioxide production (VCO2, L/min) at rest will be measured using indirect calorimetry to calculate the rate of fat oxidation at rest (g/min).
Blood insulin concentrationAt 0, 30, 60, 90 and 120min of the oral glucose tolerance test at day 7 and day 14Blood insulin concentration will be assessed in blood samples taken during the oral glucose tolerance test.
Blood fatty acid concentrationAt 0, 30, 60, 90 and 120min of the oral glucose tolerance test at day 7 and day 14Blood fatty acid concentration will be assessed in blood samples taken during the oral glucose tolerance test.
Blood glucose concentrationAt 0, 30, 60, 90 and 120min of the oral glucose tolerance test at day 7 and day 14Blood glucose concentration will be assessed in blood samples taken during the oral glucose tolerance test.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026