NCT06739564

Brief Summary

Recovery is a crucial aspect of soccer training. It has been investigated scientifically, but some unclear aspects remain regarding the optimal strategy. Recovery from maximal effort involves both physical and psychological/perceptual aspects (pain, sleep quality), and the definition of recovery is often misleading due to the subjective and objective factors involved. This is a randomized control trial comparing dry needling (DN) to ice packing (ICE) in the acute recovery after an exhaustion running trial in thirty-nine semi-professional soccer players compared to controls. The subjects were assessed before and after the exhaustion tests for sleep, pain perception (Pressure Pain Threshold, PPT), Counter Movement Jump (CMJ), and Surface Muscle Temperature (SMT). We tested 39 semi pro soccer players (males and females).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
39

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 3, 2024

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

December 3, 2024

Completed
15 days until next milestone

First Posted

Study publicly available on registry

December 18, 2024

Completed
Last Updated

December 18, 2024

Status Verified

December 1, 2024

Enrollment Period

6 months

First QC Date

December 3, 2024

Last Update Submit

December 17, 2024

Conditions

Keywords

fatiguerecoverysoccerpain threshold

Outcome Measures

Primary Outcomes (5)

  • Surface muscle temperature in degrees Centigrades.

    SMT was measured after the exhaustion trial, and after the recovery procedures. After the exhaustion trial, DN and ICE were performed. Ice packs were applied to the quadriceps, hamstrings, and soleus/gastrocnemius muscles for 20 minutes, and DN was performed by inserting the needles at relevant trigger points of the lower limb. PPT was measured before and after the recovery procedures with an FPX50 pressure gauge (Wagner, USA) on the left and right quadriceps, gastrocnemius medialis, and lateralis. SMT was measured immediately after ICE and DN in a time frame of 20 minutes from the beginning on test to the end. Final data will be reported in 3 months.

    acute, after a few minutes (20) the data are available. It will be reported in 3 months from the measurement ending.

  • Pressure pain threshold in algometer units scale.

    PPT was measured before and after the recovery procedures with an FPX50 pressure gauge (Wagner, USA) on the left and right quadriceps, gastrocnemius medialis, and lateralis. Time frame: this outcome is evaluated after 20 minutes. Final data will be reported in 3 months. Final data will be reported in 3 months.

    acute, after a few minutes (20) the data are available. It will be reported in 3 months from the measurement ending.

  • Squat Jump in cm

    A maximal Counter Movement Jump (CMJ) test (best of 3 trials) was recorded with a video analysis app (My Jump Lab, v.4.2.6). Time frame: this outcome is evaluated after 30 min from the termination of the test and before the fatigue test. Final data will be reported in 3 months.

    acute, after a few minutes (20) the data are available. It will be reported in 3 months from the measurement ending.

  • Perceived effort in RPE scores

    Borg Rate Perceived Excerption (Scale 20 level: higher the level higher the perceived effort) was measured two times, after the VO2max and after the exhaustion test at 3 and 5 minutes, and the highest value was retained. Evaluated after 1 minutes from the termination of fatigue test. Final data will be reported in 3 months.

    acute, after a few minutes (20) the data are available. It will be reported in 3 months from the measurement ending.

  • Lactate in mm/L (millimoles x liter)

    Lactate (Lactate Pro, Germany) was measured two times, after the VO2max and after the exhaustion test at 3 and 5 minutes, and the highest value was retained. Lactate was used to assess the consistency of the exhaustion trial. Lactate was evaluated at 3 and 5 minutes after the ending of the exhaustion test. Final data will be reported in 3 months.

    acute, after a few minutes (20) the data are available. It will be reported in 3 months from the measurement ending.

Study Arms (3)

Dry needling

EXPERIMENTAL

Dry needling on lower limbs

Procedure: DRY NEEDLING

Ice packing

EXPERIMENTAL

ice packing on lower limbs

Procedure: ICE PACKING

controls

NO INTERVENTION

control group

Interventions

ICE PACKINGPROCEDURE

ICE PACKING ON LOWER LIMB AFTER AN EXHAUSTION EFFORT.

Ice packing
DRY NEEDLINGPROCEDURE

DRY NEEDLING ON LOWER LIMB AFTER AN EXHAUSTION TRIAL

Dry needling

Eligibility Criteria

Age19 Years - 22 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • not having ongoing or past muscular illness in the last three months and regularly take part in training at least 5 times per week.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shanghai Tongji University

Shanghai, China, 200092, China

Location

Related Publications (1)

  • You S, Shen Y, Liu Q, Cicchella A. Patellofemoral Pain, Q-Angle, and Performance in Female Chinese Collegiate Soccer Players. Medicina (Kaunas). 2023 Mar 16;59(3):589. doi: 10.3390/medicina59030589.

    PMID: 36984590BACKGROUND

MeSH Terms

Conditions

Fatigue

Interventions

Dry Needling

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeuticsPhysical Therapy Modalities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 3, 2024

First Posted

December 18, 2024

Study Start

March 1, 2024

Primary Completion

August 31, 2024

Study Completion

November 3, 2024

Last Updated

December 18, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

PRIVACY

Locations