Skip to main content
Clinical Trials/NCT06046430
NCT06046430
Completed
Not Applicable

Investigation of Laterality and Sensory Acuity Abilities of Frozen Shoulder Patients

Harran University1 site in 1 country49 target enrollmentJanuary 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Frozen Shoulder
Sponsor
Harran University
Enrollment
49
Locations
1
Primary Endpoint
Right-Left Discrimination
Status
Completed
Last Updated
last year

Overview

Brief Summary

The brain contains the body representation necessary for normal functioning, including goal-directed movements and behaviors. Body representation involves integrated sensory input and ideas about one's body. Both executed and imagined movements depend on the representation of the body in the cortical area. Laterilization is one of the motor imagery methods that requires activation of proprioceptive, somatosensory and premotor regions and enables the determination of pain-induced cortical changes. Another method to determine pain-related somatosensory changes is the two-point discrimination test.

It is suggested that laterization and sensory acuity responses may change due to long-term pain and stiffness experienced in people with frozen shoulders. Therefore, the aim of this study is to investigate the laterization and sensory acuity abilities of patients with frozen shoulder.

Registry
clinicaltrials.gov
Start Date
January 1, 2024
End Date
August 15, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Zeynal Yasacı

Principal Investigator

Harran University

Eligibility Criteria

Inclusion Criteria

  • Patients with shoulder pain of at least six months' duration secondary to tendinopathy and/or partial rotator cuff tear; Patients with ability to follow simple orders; iii) Patients with ability to sign to provide informed consent

Exclusion Criteria

  • Normal passive ROM External ROM \< 30 To have received treatment (physiotherapy, intra-articular injection, surgery) related to the existing complaint Pain \< 3 according to the numbered pain assessment scale
  • Healthy group :
  • Inclusion criteria:
  • No actual shoulder pain or previous history of shoulder complaints including Frozen Shoulder.

Outcomes

Primary Outcomes

Right-Left Discrimination

Time Frame: Baseline

Right-Left Discrimination will be assessed with Recognise™ application. It tests the patients' ability to quickly and accurately recognise an image of a body area as either left or right ('Left/Right Discrimination'). The test will be repeated three times and average values will be recorded.

Acuity

Time Frame: Baseline

Two point discrimination is the ability to discern that two nearby objects touching the skin are truly two distinct points, not one.In clinical settings, two-point discrimination is a widely used technique for assessing tactile perception. It relies on the ability and/or willingness of the patient to subjectively report what they are feeling and should be completed with the patient's eyes closed. Aesthesiometer is the instrument used to determine two point discrimination values.

Secondary Outcomes

  • Pain Intensity(Baseline)
  • Active Range of Motion (AROM) Assessment(Baseline)
  • Central sensitization(Baseline)
  • Pain Catastrophizing(Baseline)
  • Anxiety and Depression(Baseline)

Study Sites (1)

Loading locations...

Similar Trials