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The Effects of Various High-Intensity Combined Resistance and Aerobic Training on Physical and Perceptual Outcomes in Recreationally Active Adults.

Not Applicable
Conditions
Muscular Strength
Cardiorespiratory Fitness
Physical Activity Behaviours
Healthy, recreationally active adults
Perceptual Responses to Exercise
Hormonal responses to exercise
Musculoskeletal - Normal musculoskeletal and cartilage development and function
Cardiovascular - Normal development and function of the cardiovascular system
Metabolic and Endocrine - Normal metabolism and endocrine development and function
Mental Health - Studies of normal psychology, cognitive function and behaviour
Registration Number
ACTRN12624000556549
Lead Sponsor
niversity of Technology Sydney
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
58
Inclusion Criteria

Apparently healthy, recreationally active adults that have been participating in at least 30 minutes of moderate or 20 minutes of vigorous activity on at least 3 days per week for the last 6 months. At least 1 of these training sessions must be resistance training (e.g., lifting weights, bodyweight training). This is to ensure participants are accustomed to both aerobic and resistance exercise stimuli (at a level reaching physical activity guidelines) to account for the possible confounding effects of training status. 6 months was chosen as the minimum participation duration to be currently recreationally active as this is reflects a time period where individuals have participated long enough to experience possible health benefits. Approximately 50% of participants drop out within the first 6 months.
-Aged 18-65 years.
-Male and female.
-This study welcomes participants from Indigenous Australian backgrounds, those who identify as LGBTIQ+ and those form culturally and linguistically diverse backgrounds.
-Willingness to refrain from participating in additional forms of high-intensity activity or resistance exercise during the study (e.g., competitive or social sport, other group training, other high-intensity aerobic or resistance exercise),
-Willingness to give written informed consent and willingness to participate to and comply with the study.

Exclusion Criteria

-Clinical populations (i.e., individuals requiring assessment and clearance to exercise by a health professional such as a general practitioner or exercise physiologist due to their condition or pathology) will be excluded.
-Individuals with metabolic or chronic disease, musculoskeletal injuries will be excluded.
-Individuals undergoing pharmacological treatment for psychological disorders will be excluded.
-Pregnant women will also be excluded.
-Individuals who participate in competitive/ recreational sport or training will be excluded as participants will be asked to refrain from additional high-intensity aerobic and/ or resistance exercise during the study.
-Anti-inflammatory and/or pharmacological treatment as this may interfere with inflammatory and metabolic blood markers and exercise adaptations. Exclusion based on these treatments will be done on a case-by-case basis. Treatments will be identified in the health pre-screening and participants will be excluded if there is evidence linking the treatment to changes in the physical and mental health markers that will be measured in this study.
-Contraindications to exercise as identified in the health pre-screening (Exercise and Sports Science Australia, Adult pre-exercise screening tool) (ESSA APSS).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Muscular Strength (lower body)[One repetition maximum (barbell parallel back squat) Baseline (testing day 1) after 7-weeks training (testing day 1)];Muscular strength (upper body)[One repetition maximum (barbell flat bench press) Baseline (testing day 1) after 7-weeks training (testing day 1)]
Secondary Outcome Measures
NameTimeMethod
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