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Exercise Periodization and Older Adults

Effects of Resistance Training Periodization on Hemodynamic, Morphofunctional and Cognitive Parameters of Robust Older Women.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03443375
Enrollment
14
Registered
2018-02-23
Start date
2015-01-31
Completion date
2015-12-31
Last updated
2018-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Blood Pressure, Cognitive Decline, Physical Activity, Physical Disability, Sarcopenia

Keywords

Older adults, Physical function, Muscle mass, Short-term memory, Executive function, Blood Pressure, Resistance training, Exercise training, Periodization

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.

Interventions

OTHERPhysical exercise

The interventions proposed in the present trial were based on a safe and well-established exercise training program

Sponsors

University of Campinas, Brazil
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
60 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Changes in transfer capacity in seconds6 monthsTUG performance

Secondary

MeasureTime frameDescription
Changes in fat-free mass in kg6 monthsFat-free mass
Changes in overall cognitive capacity in points6 monthsMEEM
Changes in blood pressure in mmHg6 monthsBlood Pressure
Changes in shor-term memory in points6 monthsMemory

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026