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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02842593
Other study ID # REB 14-333-1
Secondary ID
Status Completed
Phase N/A
First received July 15, 2016
Last updated January 13, 2017
Start date September 2014
Est. completion date August 2016

Study information

Verified date January 2017
Source McMaster University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the effects of two types of resistance exercise training (higher-repetition, lower load vs lower-repetition, higher load vs control) on regional and local measures of arterial stiffness in trained young men.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 2016
Est. primary completion date August 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Male

- Aged 18-30 years old

- Non-obese (Body mass index less than 30 kg/m2)

- Non-smoker

- Healthy based on questionnaire responses

- Resistance trained (Resistance training > 2 times per week for 2 years, minimum 1 lower body exercise session per week)

Exclusion Criteria:

- Allergies to milk proteins (whey or casein)

- Any acute or chronic illness, cardiac, pulmonary, liver, or kidney abnormalities, uncontrolled hypertension, insulin- or non-insulin dependent diabetes or other metabolic disorders-all ascertained through medical history screening questionnaires

- Arthritic conditions

- Individuals who consume any analgesic or anti-inflammatory drug(s), prescription or non- prescription, chronically will be excluded

- A history of neuromuscular problems

- Individuals on any medications known to affect protein metabolism (i.e. corticosteroids, non-steroidal anti-inflammatories, or prescription strength acne medications).

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Lower-repetition, heavier-load
8-12 reps/set at ~80% 1 repetition maximum
Higher-repetition, lighter-load
20-25 reps/set at ~30% 1 repetition maximum

Locations

Country Name City State
Canada McMaster University Hamilton Ontario

Sponsors (1)

Lead Sponsor Collaborator
McMaster University

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Carotid-femoral pulse wave velocity Assessed using applanation tonometry 12 weeks post exercise training
Secondary Common carotid artery distensibility Assessed using vascular ultrasound 12 weeks post exercise training
Secondary Left ventricular mass Assessed using standard echocardiography 12 weeks post exercise training
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