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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05928130
Other study ID # IDAFISAD 64202
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 30, 2023
Est. completion date February 20, 2024

Study information

Verified date March 2024
Source Universidad de Granada
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to compare the effects of different volumes of plyometric training on lower limb muscle strength, power, and muscle activity in sedentary individuals. The main question[s] it aims to answer are: - What is the minimum volume of plyometric training that can induce changes in lower limb strength and power variables? - How does muscle activity in the lower limbs vary with different volumes of plyometric training? Participants will be asked to: - Complete questionnaires to determine their level of physical activity. - Attend pre and post-evaluations of lower limb muscle activity, strength, and power during an instrumented sit-to-stand test. - Perform lower limb plyometric exercises, such as jumps, hops, and bounds. - Attend supervised training sessions three times a week for a duration of 4 weeks. Researchers will compare three groups to see if the minimum volume of plyometric training can be identified.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date February 20, 2024
Est. primary completion date January 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Subjects without lower limb musculoskeletal injuries in the past six months. - Without previous lower limb surgery in the past two years - Being sedentary Exclusion Criteria: - Medical conditions that could compromise their participation (including cardiovascular disease).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
plyometric training protocol
The plyometric training program will last for 4 weeks, with three sessions per week. The plyometric exercises will be performed immediately after a warm-up. The program will incorporate bilateral, unilateral, acyclic, cyclic, horizontal, vertical, lateral, and diagonal movements involving both slow and fast movements. Each session will include 4-5 plyometric exercises, with 2-10 sets per exercise and 1-10 repetitions per set. The training volume will progressively increase from the 1st to the 2nd week and then the intensity will increase while the volume decreases from the 3rd to the 4th week in both intervention groups. However, the final volume will vary by 50% between the groups.

Locations

Country Name City State
Chile Universidad San Sebastián, sede Valdivia. Valdivia

Sponsors (1)

Lead Sponsor Collaborator
Rodrigo Lizama Perez

Country where clinical trial is conducted

Chile, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline muscle strength at 4 weeks level of lower limb muscle strength during an instrumented sit to stand test Baseline (pre-intervention), and two days after the last training session
Primary Change from baseline muscle power at 4 weeks level of lower limb muscle power during an instrumented sit to stand test Baseline (pre-intervention), and two days after the last training session
Primary Change from baseline muscle activity at 4 weeks level of lower limb electromyographic activity during an instrumented sit to stand test Baseline (pre-intervention), and two days after the last training session
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