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High-Speed Resistance Training Program in Independent Older Adults

Primary Purpose

Old Age; Atrophy, Aging

Status
Active
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Experimental group
Sponsored by
University of Évora
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Old Age; Atrophy focused on measuring Aging, Older adults, Resistance training, Velocity-based training, Health outcomes, Phase Angle, Gait Variability

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Participants of both genders;
  • Aged 65 years old or more;
  • Can walk and perform daily tasks independently and autonomously.

Exclusion Criteria:

  • People with cognitive impairment;
  • People with neurodegenerative diseases;
  • People with diabetes disease;
  • People with heart/respiratory pathology or use of pacemakers;
  • People with musculoskeletal injuries in the 6 months before the study;
  • People with active oncology disease;
  • People with an uncontrolled hypertension (>90 mmHG; >150 mmHg);
  • People participate in other supervised exercise program;
  • Paeople who refuse to sign the informed consent.

Sites / Locations

  • Department of Sport and Health, School of Health and Human Development, University of Évora

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Experimental group

Control group

Arm Description

Participants perform a 16-week of High-Speed Resistance Training program.

Participantes continued their usual activity without engaging in any strength training or beginning a new exercise program during the study.

Outcomes

Primary Outcome Measures

Phase angle from bioelectrical impedance
Changes related to cellular health assessed by In Body S10 after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Gait Variability
Changes related to gait variability by Phypox after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.

Secondary Outcome Measures

Body Composition - Muscle mass; Fat Mass; Body Water.
Changes related to muscle mass, fat mass and body water assessed by In Body S10 and DXA after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Bone Densitometry - Whole-body BMC and BMD and dominant femoral neck BMC and BMD.
Changes related to bone quality assessed by DXA after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Heart Rate Variability
Changes related to autonomous nervous system assessed by Kubios HRV after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Physical Function
Changes related to physical function assessed by four functional fitness tests, namely 30s chair-stand; timed-up & go test; ball throw and 6 min walk test after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Muscle strength
Changes related to Muscle strength assessed by handgrip test (both sides) and isokinetic dynamometer evaluation (both sides) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Postural control
Changes related to postural control assessed in two conditions (with one foot on the ground and both feet on the ground) by an force platform Add-on (Plux) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Falls Efficacy Scale - International (FES-I)
Changes related to the level of concern about falling during social and physical activities inside and outside the home through a scale (FES-I) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
International Physical Activity Questionnaire (IPAQ)
Changes related to the levels of physical activity through a scale (IPAQ) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Mini-Mental State Examination
Changes related to the cognitive impairment (problems with thinking, communication, understanding and memory) through a scale (MMSE) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
The 36-Item Short Form Survey (SF-36)
Changes related to the health status through a scale (SF-36) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.

Full Information

First Posted
October 4, 2022
Last Updated
September 12, 2023
Sponsor
University of Évora
Collaborators
Polytechnic Institute of Rio Maior, Comprehensive Health Research Centre, CIEQV - Life Quality Research Center, Foundation for Science and Technology, Portugal
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1. Study Identification

Unique Protocol Identification Number
NCT05586087
Brief Title
High-Speed Resistance Training Program in Independent Older Adults
Official Title
Effects of an High-Speed Resistance Training Program on Health Parameters in Independent Older Adults: a Longitudinal Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 1, 2021 (Actual)
Primary Completion Date
January 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Évora
Collaborators
Polytechnic Institute of Rio Maior, Comprehensive Health Research Centre, CIEQV - Life Quality Research Center, Foundation for Science and Technology, Portugal

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The aims of the present investigation are: a) to determine the effects of a 16-weeks high-speed resistance training program on health parameters in independent older adults; and b) to verify the durability of the effects after 6 and 12 months after the intervention.
Detailed Description
The present investigation will last a total of 18 months. More specifically, Two weeks for initial assessments, then the 16-weeks training program. After that, there will be a 1-year follow-up. Regarding the training program, it consists in a high-speed resistance training program of 16-weeks, with three sessions per week (Mondays, Wednesdays, and Fridays) of 50-60min, each session being comprised of five-six exercises, two-three sets, and six-ten reps/exercise. The following exercises are used during the intervention period in pneumatic machines: incline bench press, squat in multipower or with dumbbell, leg extension, seated low row, leg press, calf raise, chest fly and lat pull down. The intensity is gradually increased after each session in accordance with the movement velocity (>1.3 to 0.75 m/s) representing approximately 20% to 60% of one repetition maximum. Participants execute the exercises rapidly and explosively making all repetitions for each shortening phase (concentric phase) performed as quickly as possible with the lengthening phase of the muscle (eccentric phase) being controlled for 2-3 s. The velocity of the concentric phase in each exercise is monitored through a BEAST™ sensor (Beast Technologies, Brescia, Italy). Participants unavailable to participate in the intervention period will be allocated to the control group. These participants continue their usual activity without engaging in any resistance training or beginning a new exercise program during the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Old Age; Atrophy, Aging
Keywords
Aging, Older adults, Resistance training, Velocity-based training, Health outcomes, Phase Angle, Gait Variability

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
88 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Participants perform a 16-week of High-Speed Resistance Training program.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Participantes continued their usual activity without engaging in any strength training or beginning a new exercise program during the study.
Intervention Type
Other
Intervention Name(s)
Experimental group
Intervention Description
The High-Speed Resistance Training program has 16 weeks, with three sessions per week with 50-60min, each session being comprised of five-six exercises, two-three sets, and six-ten reps/exercise. The intensity is gradually increased after each session in accordance with the movement velocity (>1.3 to 0.75 m/s) representing approximately 20% to 60% of one repetition maximum. Participants execute the exercises rapidly and explosively making all repetitions for each shortening phase (concentric phase) performed as quickly as possible with the lengthening phase of the muscle (eccentric phase) being controlled for 2-3 s. The velocity of the concentric phase in each exercise is monitored through a BEAST™ sensor (Beast Technologies, Brescia, Italy).
Primary Outcome Measure Information:
Title
Phase angle from bioelectrical impedance
Description
Changes related to cellular health assessed by In Body S10 after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Gait Variability
Description
Changes related to gait variability by Phypox after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Body Composition - Muscle mass; Fat Mass; Body Water.
Description
Changes related to muscle mass, fat mass and body water assessed by In Body S10 and DXA after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Bone Densitometry - Whole-body BMC and BMD and dominant femoral neck BMC and BMD.
Description
Changes related to bone quality assessed by DXA after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Heart Rate Variability
Description
Changes related to autonomous nervous system assessed by Kubios HRV after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Physical Function
Description
Changes related to physical function assessed by four functional fitness tests, namely 30s chair-stand; timed-up & go test; ball throw and 6 min walk test after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Muscle strength
Description
Changes related to Muscle strength assessed by handgrip test (both sides) and isokinetic dynamometer evaluation (both sides) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Postural control
Description
Changes related to postural control assessed in two conditions (with one foot on the ground and both feet on the ground) by an force platform Add-on (Plux) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Falls Efficacy Scale - International (FES-I)
Description
Changes related to the level of concern about falling during social and physical activities inside and outside the home through a scale (FES-I) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
International Physical Activity Questionnaire (IPAQ)
Description
Changes related to the levels of physical activity through a scale (IPAQ) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
Mini-Mental State Examination
Description
Changes related to the cognitive impairment (problems with thinking, communication, understanding and memory) through a scale (MMSE) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months
Title
The 36-Item Short Form Survey (SF-36)
Description
Changes related to the health status through a scale (SF-36) after a 16-weeks high-speed resistance training program and after 6 and 12 moths of the intervention period.
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Participants of both genders; Aged 65 years old or more; Can walk and perform daily tasks independently and autonomously. Exclusion Criteria: People with cognitive impairment; People with neurodegenerative diseases; People with diabetes disease; People with heart/respiratory pathology or use of pacemakers; People with musculoskeletal injuries in the 6 months before the study; People with active oncology disease; People with an uncontrolled hypertension (>90 mmHG; >150 mmHg); People participate in other supervised exercise program; Paeople who refuse to sign the informed consent.
Facility Information:
Facility Name
Department of Sport and Health, School of Health and Human Development, University of Évora
City
Évora
ZIP/Postal Code
7004-516
Country
Portugal

12. IPD Sharing Statement

Plan to Share IPD
No

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High-Speed Resistance Training Program in Independent Older Adults

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