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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03645772
Other study ID # S60983
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 29, 2018
Est. completion date June 19, 2018

Study information

Verified date August 2018
Source KU Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Rapid force production declines as a consequence of ageing. Given the functional relevance of rapid force production, exercise interventions in older adults should aim at improving the capacity to produce force rapidly. To improve this capacity, exercises should be performed with the intention to develop high speeds, as supported by previous work.

Human locomotion fundamentally consists of multi-joint movements and rapidly coupled eccentric-concentric muscle actions, known as stretch-shortening cycle (SSC) activities or plyometrics. Plyometrics might therefore be used to optimize power production. However, there is limited research on the feasibility of plyometrics in older adults and its potential effects on rapid force production and functional capacity. This study will test the feasibility of a 12-week plyometric exercise intervention in older men and compare its effects on rapid force production to a traditional resistance exercise or walking intervention.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date June 19, 2018
Est. primary completion date June 19, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 65 Years to 80 Years
Eligibility Inclusion Criteria:

Exclusion Criteria:

- No systematic engagement in (resistance) exercise in the 12-months prior to participation

- Cardiovascular disease

- Neurological disorders

- Cognitive malfunctioning

- Severe knee or hip problems

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise intervention
12-week progressive training intervention

Locations

Country Name City State
Belgium Department of Movement Sciences Leuven

Sponsors (1)

Lead Sponsor Collaborator
KU Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rapid force production Subjects perform a test protocol on a sledge apparatus, consisting of explosive isometric voluntary contractions for the leg-extensor muscles of the right leg. The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). The knee joint angle is set at 90° and the hip angle at 70°. The point of force application is aligned with the head of the fifth metatarsal. Subjects are instructed to kick as fast and as hard as possible and maintain their maximum force for approximately 3s. The rate of force development (N/s) is defined as the linear slope of the force-time curve and is measured from the onset of movement till 100 ms. Change from baseline in rapid force production at 12 weeks
Primary Jumping height in squat jump Subjects perform a test protocol on a sledge apparatus, consisting of squat jumps (SJ), countermovement jumps (CMJ), and drop jumps (DJ). The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). A force platform is built in perpendicular to the jumping direction. A speed sensor is attached to the seat of the sledge, which is used to assess the transition point between braking and push-off phases and to calculate jumping height (in cm). Change from baseline in jumping height at 12 weeks
Primary Jumping height in countermovement jump Subjects perform a test protocol on a sledge apparatus, consisting of squat jumps (SJ), countermovement jumps (CMJ), and drop jumps (DJ). The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). A force platform is built in perpendicular to the jumping direction. A speed sensor is attached to the seat of the sledge, which is used to assess the transition point between braking and push-off phases and to calculate jumping height (in cm). Change from baseline in jumping height at 12 weeks
Primary Jumping height in drop jump Subjects perform a test protocol on a sledge apparatus, consisting of squat jumps (SJ), countermovement jumps (CMJ), and drop jumps (DJ). The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). A force platform is built in perpendicular to the jumping direction. A speed sensor is attached to the seat of the sledge, which is used to assess the transition point between braking and push-off phases and to calculate jumping height (in cm). Change from baseline in jumping height at 12 weeks
Secondary Leg press one-repetition maximum Leg press one-repetition maximum is defined as the maximum weight (in kg) that the subject can push on a leg press device (Signature Series Leg press Life Fitness). Change from baseline in leg press 1-RM at 12 weeks
Secondary Maximal isometric strength Maximal strength (Nm) is measured by means of unilateral isometric knee-extensor tests on a Biodex dynamometer. Change from baseline in maximal isometric strength at 12 weeks
Secondary Maximal isokinetic strength Maximal strength (Nm) is measured by means of unilateral isokinetic knee-extensor tests on a Biodex dynamometer. Change from baseline in maximal isokinetic strength at 12 weeks
Secondary Stair Climbing performance Stair ascent duration (in s), the time needed to ascent a flight of stairs. Change from baseline in Stair Climbing performance at 12 weeks
Secondary Gait speed The average speed to walk 10m as fast as possible (in m/s). Change from baseline in gait speed at 12 weeks
Secondary 5 repetition sit-to-stand test The time needed to perform 5 sit-to-stand transitions (in s). Change from baseline in sit-to-stand duration at 12 weeks
Secondary 6 minute walk distance The walk distance (in m) covered in 6 min. Change from baseline in 6min walk distance at 12 weeks
Secondary Balance Overall balance performance is assessed using the total length of the sway path divided by duration of the measurement (mm/s) in a 30s balance test on a balance board. Change from baseline in balance at 12 weeks
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