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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04053920
Other study ID # 236559
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2018
Est. completion date December 18, 2019

Study information

Verified date March 2020
Source University of Glasgow
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the current study, therefore, is to determine the feasibility of recruitment and adherence to resistance exercise training interventions performed at low and high loads, to volitional muscular failure, in a trial population that includes both healthy and frail older people.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 18, 2019
Est. primary completion date December 18, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Over age of 65 years

Exclusion Criteria:

- Current participation in an exercise programme

- Exercise deemed unsafe by clinical team

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Low Load Resistance exercise
leg extension, leg press, leg curl and calf press
High Load Resistance exercise
leg extension, leg press, leg curl and calf press

Locations

Country Name City State
United Kingdom GRI Clinical Research Facility Glasgow

Sponsors (1)

Lead Sponsor Collaborator
University of Glasgow

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle strength Knee extensor maximal torque during an isometric MVC Change from baseline to 8 weeks
Secondary Vastus lateralis muscle thickness Measured via ultrasound Change from baseline to 8 weeks
Secondary Muscle strength Knee flexor maximal torque during an isometric MVC Change from baseline to 8 weeks
Secondary One-repetition maximum leg extension, leg curl, leg press and calf press Change from baseline to 8 weeks
Secondary Biomechanics during walking and stair climbing Motion analysis Change from baseline to 8 weeks
Secondary Short performance physical battery test SPPB - balance, walking pace and chair rise Change from baseline to 8 weeks
Secondary Quality of life measure EQ-5D-5L questionnaire Change from baseline to 8 weeks
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