CClinicalTrials.gg
Not yet recruitingNCT06747104Updated Dec 24, 2024

Application of Manual Therapy to Archers

An interventional study of Manual therapy and Placebo in Healthy, sponsored by Medical University of Gdansk. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-12-24.

Sponsored by Medical University of Gdansk · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 9 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to: (i) characterize the effect of repeated archery shots on the EMG parameters of certain selected upper limb muscles; and (ii) evaluate how manipulation of the initial two-second tension phase, in particular involving muscle stretching, affects these EMG parameters after repeated shots.

Read the detailed description

EMG measurements will be collected for selected muscles in the shoulder joint and forearm, at points: initially at the beginning, after the athletes have performed 50 and another 50 archery shots, and finally after undergoing manual therapy. The main phase of muscle testing will take place in the Aiming phase.

02

Conditions studied

  • Healthy

Keywords

  • archery
  • muscle fatigue
  • recovery
  • manipulation
03

In context

Lead sponsor

Medical University of Gdansk is the lead sponsor of 130 studies on the registry; 46 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Actively training as an archer at least twice a week for six months;
  • In good health, with no recent injury or illness;
  • Over 18 years of age;
  • Engagement in all phases of the study.

Exclusion criteria

Exclusion Criteria:

  • Any injury or illness present at the time of the study;
  • Recent history (within six months) of upper extremity injury (shoulder, elbow, or wrist), joint pain, lower extremity joint hypermobility, or neurological/connective tissue disease.
  • No training participation
  • No consent for study
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Active comparator
    Assessment of acute effects of manipulation and muscle strength

    Performing the manipulation with a preliminary two-second tension of the joint capsule in the shoulder and elbow joints.

    Other: Manual therapy · Other: Placebo

Interventions

  • OtherManual therapy

    This technique involves a low-amplitude, high-velocity push on the shoulder and elbow joints with an additional two-second tension

  • OtherPlacebo

    Performing manipulations without a two-second preliminary tension of the joint capsule in the shoulder and elbow joints.

06

What researchers measure

Primary outcomes

  1. Assessment of MVC.

    Muscle EMG is an assessment of the electrical characteristics during the study, the electrical source of which is the muscle membrane potential, and the measured EMG potentials are measured in μV and the repetition rate of muscle motor unit firing measured in Hz, at the same time of the study.

    Time frame: Each isometric muscle test lasts 3 seconds. The study is performed three times for each muscle.

  2. Muscle stiffness

    Muscle stiffness - characteristic resistance to physical contraction, which deforms initially forming. Stiffness (N/m) was calculated as S = amax.mprobe/Δl.

    Time frame: Each Myoton application lasts 1 sec for one point. Three evaluations of one of the two points for one muscle are performed. It is assumed that the study with recording will last 30 seconds for one muscle.

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Once the study is complete, the results will be sent to the researcher who will analyze the data.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 24, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06747104
Lead sponsor
Medical University of Gdansk
Responsible party
Sponsor
First posted
Dec 24, 2024
Start date
Dec 10, 2024 (estimated)
Primary completion
Dec 31, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Dec 24, 2024

Study contacts

Rafał Studnicki, PhD
Contact
fizjoterapia@gumed.edu.pl
+48583491509
Rafał Studnicki, PhD
principal investigator · Medical University of Gdansk

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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