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Clinical Trials/NCT06226961
NCT06226961CompletedNot Applicable

Immediate Effects of Dynamic Cupping on Shoulder Active Range of Motion of Senior Male Handball Athletes: A Randomized Controlled Trial

University Fernando Pessoa2 sites in 1 country80 target enrollmentStarted: February 2, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
80
Locations
2
Primary Endpoint
active movements of the shoulder

Study Overview

Brief Summary

The purpose of this study is to to verify the immediate effects of dynamic cupping on shoulder active range of motion (AROM) of senior male handball athletes.

Detailed Description

After completing the questionnaire, 80 senior male handball athletes will be randomly divided into two designated groups, Intervention Group (IG; n = 40) (dynamic cupping therapy) and Control Group (CG; n = 40) (no intervention).

Shoulder AROM (flexion, extension, abduction, adduction, horizontal adduction, horizontal abduction, internal rotation and external rotation movements) will be assessed in both control and intervention groups before (M0) and after (M1) intervention.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 39 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Healthy senior handball athletes in competition with at least three training sessions per week.

Exclusion Criteria

  • history of injury, fracture or surgical intervention in the upper limb in the last six months before the study;
  • vestibular, neurological or cardiorespiratory diseases;
  • reported pain in the upper limb or spine
  • presence of contraindication for cupping (deep venous thrombosis, with active infection or open wound.

Outcomes

Primary Outcomes

active movements of the shoulder

Time Frame: [Time Frame: Change from Baseline (M0) to Immediately after intervention or control (M1)]

Data will be collected in two moments: baseline (M0) and after the intervention/control (M1). The shoulder range of motion will be measured using a universal goniometer. Participants will be instructed to perform the various active movements of the shoulder on the dominant upper limb. The assessments of the shoulder flexion, extension, abduction and adduction movements will be performed standing up, controlling possible compensations. To assess abduction and horizontal adduction movements, the participants will remain seated on a massage table. Internal and external rotation movements will be assessed on a massage table in supine, without inclination. Measurements will be considered invalid if the participant is compensated with another body part. Three measures will be collected for each movement and the average of the three will be considered.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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