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Clinical Trials/NCT07334171
NCT07334171
Completed
Not Applicable

Inspiratory Muscle Strength and Diaphragm Thickness in Tennis Players With and Without Shoulder Pain: A Case-Control Study

Universidad Francisco de Vitoria1 site in 1 country64 target enrollmentStarted: February 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Universidad Francisco de Vitoria
Enrollment
64
Locations
1
Primary Endpoint
Maximal Inspiratory Pressure (MIP)

Overview

Brief Summary

This observational case-control study will compare inspiratory muscle function and diaphragm morphology between individuals with shoulder pain and asymptomatic controls. Participants will be allocated into two groups according to the presence or absence of shoulder pain.

Inspiratory muscle strength will be assessed by measuring maximal inspiratory pressure (MIP) using standardized procedures. Diaphragm thickness will be evaluated bilaterally using ultrasound imaging at the end of inspiration (Tins) and at the end of expiration (Texp).

Pain intensity will be assessed using the Visual Analog Scale (VAS). Upper limb disability will be evaluated using the QuickDASH questionnaire, including the activities of daily living module and the optional sports module.

All outcomes will be assessed in a single evaluation session. Between-group comparisons will be performed to analyze differences in inspiratory muscle strength, diaphragm thickness, pain intensity, and upper limb disability between participants with and without shoulder pain.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Tennis player who suffered from non-specific shoulder pain
  • Training at least two times per week
  • Have experienced at least 1 episode of non-specific shoulder pain in the last month
  • A positive result on the following diagnostic tests: Neer Test and Jobe Test

Exclusion Criteria

  • Having taken anti-inflammatories or muscle relaxants within the last 72 hours before the study
  • Pregnancy
  • Previous diagnosis of respiratory or neurological diseases
  • Previous surgeries, fractures, and dislocations in the dominant shoulder
  • Inability to follow instructions during the study
  • All those for whom measuring maximum inspiratory pressure is contraindicated: unstable angina, recent myocardial infarction (within 4 weeks of the even or myocarditis, uncontrolled systemic hypertension, recent pneumothorax, post-lung biopsy surgery of less than one week, postoperative abdominal or genitourinary surgery of less than 6 months, and urinary incontinence

Arms & Interventions

Shoulder Pain Group

Participants with shoulder pain

Healthy Control Group

Participants without shoulder pain

Outcomes

Primary Outcomes

Maximal Inspiratory Pressure (MIP)

Time Frame: Single assessment at baseline visit

Maximal inspiratory pressure measured in cmH₂O using a respiratory pressure meter as an indicator of inspiratory muscle strength.

Diaphragm thickness at inspiration

Time Frame: Single assessment at baseline visit

Bilateral diaphragm muscle thickness measured by ultrasound imaging at the end of maximal inspiration (Tins)

Diaphragm thickness at expiration

Time Frame: Single assessment at baseline visit

Bilateral diaphragm muscle thickness measured by ultrasound imaging at the end of maximal expiration (Texp).

Secondary Outcomes

  • Pain intensity (VAS)(Single assessment at baseline visit)
  • Upper limb disability - activities of daily living(Single assessment at baseline visit)
  • Upper limb disability - sport(Single assessment at baseline visit)

Investigators

Sponsor
Universidad Francisco de Vitoria
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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