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Clinical Trials/NCT05397418
NCT05397418CompletedNot Applicable

Effectiveness of a 12-week Low Impact Resistance Training Programme on Muscle Function, Body Composition, Quality of Life and Muscle Protein Synthesis in Women Aged 40-60 Years

University of Exeter1 site in 1 country72 target enrollmentStarted: May 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
72
Locations
1
Primary Endpoint
Muscle function

Study Overview

Brief Summary

Participating in regular physical activity has been shown to reduce the risk of developing some diseases and disabilities that can occur with ageing. Muscles naturally decline with age, and in females this appears to occur more so around the time of menopause. Time, work, family commitments and the availability of facilities have all been identified as barriers to exercise in middle age.

Increasing activity levels in middle age appears to improve muscle function and bone health. However, there is a lack of evidence in how muscle function responds to low impact resistance exercise in middle aged females.

This study aims to assess the effectiveness and the mechanisms associated with building muscle as well as the effect on quality of life in middle aged (40-60 years) females using a low impact resistance training programme.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
40 Years to 60 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Females aged 40-60 years of age at time of screening.
  • •Body mass index <30kg/m2 and >18.5kg/m2
  • •Considered moderately active according to the 7 day International Physical Activity Questionnaire (IPAQ) (Craig et al., 2003)
  • •Self-reported as healthy (absence of injury or disease).
  • •Availability and willingness to attended 12 weeks of exercises classes 4-5 times per week at St Luke's Campus Exeter and participate in the study lasting a total of 26 weeks.

Exclusion Criteria

  • •Pregnant, lactating or planning a pregnancy.
  • •Current diagnosis of a chronic disease such as diabetes, autoimmune disease, cardiovascular disease, kidney disease.
  • •Hysterectomy and/or ovariectomy.
  • •Currently prescribed hormone replacement therapy.
  • •Hypertension (BP ≥149/90 mm/Hg)
  • •Either current smoker, or history of smoking in the past 6 months.
  • •Currently taking supplements that have been shown to impact muscle function and muscle mass, such as creatine, in the last 6 months.
  • •Prescribed medications that have been shown to impact muscle function and muscle mass, such as steroids, in the last 6 months.
  • •History of epilepsy.
  • •Current or recent injury within the last 6 months that may affect their ability to carry out the resistance training program.
  • •Advised not to exercise by their General Practitioner or medical professional.
  • •Resistance training consistently for 3 or more times per week for the last 2 months

Arms & Interventions

Intervention group

Experimental

Supervised exercise program week 1-12, unsupervised exercise week 13-24.

Intervention: Supervised resistance exercise program (Behavioral)

Intervention group

Experimental

Supervised exercise program week 1-12, unsupervised exercise week 13-24.

Intervention: Unsupervised resistance exercise program (Behavioral)

Control group

Sham Comparator

Maintain habitual activity week 1-12, unsupervised exercise week 13-24.

Intervention: Unsupervised resistance exercise program (Behavioral)

Outcomes

Primary Outcomes

Muscle function

Time Frame: 12 weeks

Peak torque (Nm) of the shoulder and hip

Secondary Outcomes

  • Muscle thickness(12 weeks)
  • Muscle protein synthesis(12 weeks)
  • Energy expenditure(12 weeks)
  • Bone mineral density(12 weeks)
  • Physical activity levels(12 weeks)
  • Exercise program acceptability(12 weeks)
  • Changes in balance(12 weeks)
  • Changes in flexibility(12 weeks)
  • Changes in diabetes risk markers(12 weeks)
  • Body composition(12 weeks)
  • Sleep Quality(12 weeks)
  • Self reported quality of life(12 weeks)
  • Changes in cardiovascular risk markers(12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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