NCT06226961

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
80

participants targeted

Target at P75+ for not_applicable healthy

Timeline
Completed

Started Feb 2024

Shorter than P25 for not_applicable healthy

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

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 17, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 26, 2024

Completed
7 days until next milestone

Study Start

First participant enrolled

February 2, 2024

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 9, 2024

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 23, 2024

Completed
Last Updated

April 9, 2024

Status Verified

January 1, 2024

Enrollment Period

7 days

First QC Date

January 17, 2024

Last Update Submit

April 7, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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)]

Study Arms (2)

Intervention group

EXPERIMENTAL

For the dynamic cupping protocol, the participants will be instructed to remain seated on the massage table with their feet supported, and the technique will applied to the entire shoulder (anterior, lateral and posterior face) and surrounding muscles (upper trapezius and pectoralis major). The cupping will be performed using a plastic cupping cup (5,08 cm in diameter) (K.S. Choi Corp®) and a pistol grip hand pump (K.S. Choi Corp®). The dynamic cupping will be performed for ten minutes, at a slow pace, and consists 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.

Device: cupping

Control group

NO INTERVENTION

Participants in the CG group will remain at rest, sitting on the massage table for 10 minutes.

Interventions

cuppingDEVICE

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.

Intervention group

Eligibility Criteria

Age18 Years - 39 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Escola Superior Saúde Fernando Pessoa

Porto, 4200-253 Porto, Portugal

Location

MeSH Terms

Interventions

Cupping Therapy

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeutics

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 17, 2024

First Posted

January 26, 2024

Study Start

February 2, 2024

Primary Completion

February 9, 2024

Study Completion

February 23, 2024

Last Updated

April 9, 2024

Record last verified: 2024-01

Locations