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High-intensity Training for Improving Physical Performance of Aged Women

Effects of High-intensity Interval Circuit Training (HIICT) on the Cardiovascular and Functional Parameters of Aged Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03840330
Acronym
AHIITATE
Enrollment
54
Registered
2019-02-15
Start date
2015-12-20
Completion date
2016-06-20
Last updated
2019-03-06

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

Conditions

Aging, Cardiovascular Risk Factor, Healthy, Physical Activity

Keywords

High-intensity interval training, Circuit training, Elderly, Functional capacity, VO2 max, Cardiovascular parameters

Brief summary

This study evaluates the adaptations on the functional capacity and cardiovascular in elderly after a physical activity program circuit training. The participants were divided into three groups: Circuit training based on high-intensity interval training group (HIICT), Circuit training at moderate intensity group (MICT) and Control group (CG).

Detailed description

Three groups of participants (circuit training based on high-intensity interval training, circuit training at moderate intensity and not training group) will enter the study. The intervention will consist of a physical exercise program in day centers. Intensity progression will be encouraged according to the rate of perceived exertion. Progression of exertion will be very hard, extremely hard and maximal exertion for HIT group, and light, somewhat hard and hard for group. Assessment will be undertaken at two-time points: baseline and after 16 weeks of exercise training. Assessment will include VO2 peak, functional capacity, health-related quality of life, cognitive state and daily physical activity.

Interventions

OTHERExperimental: High-intensity interval training group

16 weeks of High-intensity interval training

OTHERExperimental: Moderate-intensity interval training group

16 weeks of Moderate-intensity interval training

Sponsors

Universidad de Almeria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

HIT; MIT; GC

Eligibility

Sex/Gender
FEMALE
Age
50 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

1. Having 50 - 90 years old. 2. Not suffering chronic heart, respiratory or joint disease, taking medication or having a deteriorated level of mental health that could interfere in carrying out exercise programs. 3. Having 0 or 1 responses positive in the Physical Activity Readiness Questionnaire (ParQ). Only item 6, related to mild vascular diseases. 4. Being physically independent according to the scales Lawton and Brody, and Katz.

Exclusion criteria

1. Having uncontrolled arterial hypertension. 2. Having practiced during the previous 3 months or practicing at present a similar exercise to the one proposed in the study. 3. Attending sessions less than 80%.

Design outcomes

Primary

MeasureTime frameDescription
Analyses changes in maximum oxygen consumption (VO2max).Pre and post after sixteen weeks of interventionA modified Balke treadmill protocol will be used to estimate aerobic capacity (VO2max).

Secondary

MeasureTime frameDescription
Analyses changes in heart rate reached in ergometry.Pre and post after sixteen weeks of interventionAnalyses during modified Balke treadmill protocol
Analyses changes in blood pressure reached in ergometry.Pre and post after sixteen weeks of interventionAnalyses during modified Balke treadmill protocol
Analyses changes in maximum speed reached in ergometry.Pre and post after sixteen weeks of interventionAnalyses during modified Balke treadmill protocol
Analyses changes in duration test reached in ergometry.Pre and post after sixteen weeks of interventionAnalyses during modified Balke treadmill protocol
Analyses changes in fat percentage.Pre and post after sixteen weeks of intervention.Fat percentage (%) was assessed using bioimpedance analysis (OMROM BF-306).
Analyses changes in body mass index (BMI).Pre and post after sixteen weeks of intervention.BMI was assessed using bioimpedance analysis (OMROM BF-306).
Analyses changes in gait.Pre and post after sixteen weeks of intervention.Gait was assessed using the Timed Up and Go Test. To stand up from a standard arms chair, walk 3 meters, turn back the cone walk back and sit down to the chair. The time in seconds is record.
Analyses changes in balance.Pre and post after sixteen weeks of intervention.Balance was assessed using the One Leg Standing Test. This test consist in maintain one leg stance for as long as possible. The test was considered normal if the one leg standing time reached 30 seconds.
Analyses changes in lower body strength.Pre and post after sixteen weeks of intervention.Lower body strength was assessed using the Sit To Stand 30. For the Sit To Stand 30, the participant consist in measures how many repetition the participant can to stand up and sit down during 30 seconds.
Analyses changes in upper body strength.Pre and post after sixteen weeks of intervention.Upper body strength was assessed using the Arm Curl Test (30). For this test, the participant consist in measures how many repetition the participant can to curl up and curl down during 30 seconds.
Analyses changes in maximal handgrip strength.Pre and post after sixteen weeks of intervention.To measure the amount of strength developed by each hand in kg.

Other

MeasureTime frameDescription
Analyses change in Self Assessed Physical Activity.Pre and post after sixteen weeks of intervention.Physical activity was assessed using the Physical Activity Scale of the Elderly (PASE) questionnaire. The PASE is designed to assess physical activity in older persons. The total PASE score was computed by multiplying the amount of time spent in each activity (hours/week) or participation (yes/no) in an activity by empirically derived item weights and summing over all activities. PASE scores for this study ranged from 0 to 756 with higher scores indicating more physical activity.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026