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A New Shoulder Proprioceptive Rehabilitative Tool (SRPT) for the Evaluation of the Role of the Shoulder During Reaching

A New Neurocognitive Interpretation of the Shoulder Position Sense During Reaching

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02646306
Acronym
SRPT-Iphase
Enrollment
44
Registered
2016-01-05
Start date
2015-07-31
Completion date
2016-01-31
Last updated
2016-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder Impingement Syndrome

Keywords

shoulder, proprioception, movement, reaching

Brief summary

The aim of the study focused on the creation of a rehabilitative measuring device (SRPT-shoulder proprioceptive rehabilitation tool) and the development of the examination methodology for assessing the proprioception of the glenohumeral joint respect to scapula abduction, within the movement of antepulsion on the sagittal plane both in healthy subjects and in patients with shoulder impingement syndrome.

Interventions

OTHERshoulder proprioceptive rehabilitation tool

Using of this tool to measure which is the average error in reaching back in both healthy subjects and subjects with shoulder impingement syndrome starting from the assumption that the shoulder, through the articulation scapulothoracic, helps to determine direction and distance during the reaching of an object.

Sponsors

University of Roma La Sapienza
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
55 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Right-handed * Diagnosis of subacromial right impingement syndrome performed by the orthopedic specialist (nuclear magnetic resonance and/or ultrasound examination) * Neer stages 1, 2 and 3 * Presence of pain 3 \<VAS\<8 at baseline * Age between 55 and 65 years.

Exclusion criteria

* Diabetes mellitus * Inflammatory systemic diseases * CNS and/or PNS diseases * Systemic infectious diseases * Neoplastic diseases * Assumption of antidepressants and/or anxiolytics and/or other medications that can affect attention and sensory * Visual problems not properly compensated * Previous surgery to the shoulder

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of the Visual Analogue Scale (VAS) at baselinebaselineIt is an instrument that enables patients to express their pain intensity as a numerical value. Patients were asked to mark the point that corresponded to their perceived pain intensity on a 10-cm line, with 0 indicating the absence of pain and 10 reflecting the most severe pain

Secondary

MeasureTime frameDescription
Evaluation of the short form of the Disabilities of the Arm, Shoulder and Hand questionnaire (Quick-DASH) at baselinebaselineThe short form (11 item) of the Disabilities of the Arm, Shoulder and Hand questionnaire (Quick-DASH) measures physical ability and symptoms of the upper extremity and explores the impact of functional impairment and pain on daily-living tasks, as well as on social and recreational activities, work and sleep. The score ranges from 0 to 100 points, with 0 reflect- ing no disability and 100 corresponding to the most severe disability
Evaluation of the Constant-Murley shoulder outcome score at baselinebaselineIt is based on subjective (sleep, work, and recreational activities) and objective (ROM and strength) components, adjusted for age and sex, according to normative values reported by Yian et al. The score ranges from 0 (worst result) to 100 (best result).

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026