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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06226961
Other study ID # FISIO-3-29072019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2, 2024
Est. completion date February 23, 2024

Study information

Verified date January 2024
Source University Fernando Pessoa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date February 23, 2024
Est. primary completion date February 9, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 39 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
cupping
The dynamic cupping will be performed for ten minutes, at a slow pace, and consisted of applying a small amount of massage cream (ATL®) over the entire shoulder (to obtain the ideal sliding surface for cupping application), insufflation of the suction cup, with two pumps, and sliding it in the direction of the muscle fibers around the shoulder and also in the transversal direction.

Locations

Country Name City State
Portugal Escola Superior Saúde Fernando Pessoa Porto

Sponsors (1)

Lead Sponsor Collaborator
University Fernando Pessoa

Country where clinical trial is conducted

Portugal, 

Outcome

Type Measure Description Time frame Safety issue
Primary active movements of the shoulder 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.
[Time Frame: Change from Baseline (M0) to Immediately after intervention or control (M1)]
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