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Effects of Intermittent Pneumatic Compression Following Exercise-induced Muscle Damaged

Effects of Intermittent Pneumatic Compression Following Exercise-induced Muscle Damaged

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06201260
Acronym
IPC4sports
Enrollment
33
Registered
2024-01-11
Start date
2024-02-15
Completion date
2024-03-15
Last updated
2024-05-08

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

Conditions

Sports Physical Therapy

Brief summary

This study aims to assess the recovery kinetics following an exercise-induced muscle damage activity (using flywheel) on active healthy university students. The main questions are: \- Is intermittent pneumatic compression superior to a placebo recovering from EIMD? Participants will perform a fatiguing protocol using flywheel and recover with either intermittent pneumatic compression or with a placebo treatment (micro-current treatment, but the device turned off). They will perform several performance tests before, following the recovery period, and at the 24h and 48h following the intervention

Interventions

OTHERintermittent pneumatic compression protocol

A 30 min IPC protocol at about 200mmHg

OTHERPlacebo treatment

The electrodes of an electrostimulation device (SP 4.0, Compex, Guildford, United Kingdom) will be positioned on participants' quadriceps. Participants will be informed that they are engaging an innovative microcurrent treatment. This procedure will last for 30 min.

Sponsors

University of Maia
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
MALE
Age
18 Years to 27 Years
Healthy volunteers
Yes

Inclusion criteria

* To be eligible for participating in this study, participants should not have been recently injured, and should engage physical activity regularly (\>3 times/week).

Exclusion criteria

* Inactive participants * Younger than 18 years old or older than 27 years old

Design outcomes

Primary

MeasureTime frameDescription
Maximal voluntary contraction (knee extension)10 minutes before the fatigue protocol, following the recovery protocol (30 minutes post), 24 hours and 48 hours post interventionMeasures of isometric strength
Countermovement jump10 minutes before the fatigue protocol, following the recovery protocol (30 minutes post), 24 hours and 48 hours post interventionJump height
Broad Jump10 minutes before the fatigue protocol, following the recovery protocol (30 minutes post), 24 hours and 48 hours post interventionHorizontal jump
Soreness scale10 minutes before the fatigue protocol, following the recovery protocol (30 minutes post), 24 hours and 48 hours post interventionLikert scale of muscle soreness - the scale ranges from from 0 (a complete absence of soreness) to 6 (a severe pain that limits the ability to move)

Countries

Portugal

Outcome results

None listed

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