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Exercise Periodization and Older Adults

Not Applicable
Completed
Conditions
Aging
Physical Activity
Blood Pressure
Cognitive Decline
Sarcopenia
Physical Disability
Registration Number
NCT03443375
Lead Sponsor
University of Campinas, Brazil
Brief Summary

The present study aimed at investigating the effects of two different resistance training protocols - nonperiodized (NP) and daily undulating periodization (DUP) - on hemodynamic, morphofunctional and cognitive parameters of robust older women. Methods: Forty-two older women were randomized allocated into one of the three experimental groups: NP, DUP, and control group (CG). Evaluations of the hemodynamic, morphofunctional and cognitive parameters occurred before, during and after six months. The exercise groups performed the program of exercise twice a week over 22 weeks. In NP, the two weekly sessions were based on 3 sets of 8-10 repetitions at a difficult intensity. However, in DUP, a power exercise session based on 3 sets of 8-10 repetitions at a moderate intensity was added in the first session of the week.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
14
Inclusion Criteria
  • Aged ≥60 years;
  • Female;
  • Not having been part of a systematic program of physical exercises in the last 6 months;
  • MEEM score >19 points;
  • Kihon checklist score >10 points;
  • Capacity to perform the basic and instrumental activities of daily living according to Katz and Pfeffer indexes;
  • Self-reported good memory;
  • Complete all measurements.
Exclusion Criteria
  • Changes on antihypertensive medication in the past 6 months prior to inclusion in the study;
  • Cardiovascular disease (i.e., acute myocardial infarction, stroke, peripheral arterial disease, and transient ischemic disease)
  • Metabolic disease (i.e., diabetes mellitus type I or II), pulmonary disease (i.e., emphysema)
  • Neurological and/or psychiatric disease (i.e., Parkinson's or Alzheimer's disease)
  • Skeletal muscle disorders
  • Comorbidities associated with greater risk of falls
  • Recent history of smoking or alcohol abuse
  • Hormone replacement therapy and/or psychotropic drugs.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Changes in transfer capacity in seconds6 months

TUG performance

Secondary Outcome Measures
NameTimeMethod
Changes in fat-free mass in kg6 months

Fat-free mass

Changes in overall cognitive capacity in points6 months

MEEM

Changes in blood pressure in mmHg6 months

Blood Pressure

Changes in shor-term memory in points6 months

Memory

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