Effects of Cryotherapy on Joint Function and Pressure Pain Threshold in Patients With Subacromial Impingement Syndrome.

Sponsor
Universidade Federal de Sao Carlos (Other)
Overall Status
Completed
CT.gov ID
NCT02351986
Collaborator
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. (Other)
30
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18
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Study Details

Study Description

Brief Summary

Background: Subacromial impingement syndrome (SIS) is a chronic and disabling disease, characterized by compression and mechanical abrasion of the tendons of the rotator cuff muscles, subacromial bursa and tendon of the long head of the biceps against the anterior surface of the acromion, coracoacromial ligament or the acromioclavicular joint during arm elevation movement. After the trauma, inflammatory processes initiate and may lead to loss of function when untreated. This inflammation leads the release of cytokines (IL-6, IL-10, IL-1β and TNF-α) whose acts as inflammatory mediators. Physical therapy works in treating SIS with the goal of reducing pain and inflammatory process. Cryotherapy is widely used in physical therapy by anti-inflammatory and analgesic effects, low cost, effectiveness and easy application. Objective: The aim of the study is to evaluate the effects of a cryotherapy protocol, applied on shoulder of subjects with SIS, on serum inflammatory mediators (cytokines) and local pressure pain threshold. Possible changes in function and pain will also be evaluated. Materials and Methods: 30 subjects will be selected and share in two groups, 15 healthy subjects and 15 subjects with SIS. Function assessments and quality of life will be held using the DASH and WORC questionnaires. Cryotherapy will be applied for 4 consecutive days, lasting 20 minutes without interruption through ice pack over the shoulder of SIS carriers. For the blood samples, 20ml of blood will be collected at the first and last day of the intervention, and then stored at -80 ° C.

Condition or Disease Intervention/Treatment Phase
  • Procedure: physical therapy
  • Other: ice pack
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Cryotherapy on Inflammatory Mediators, Joint Function and Pressure Pain Threshold in Patients With Subacromial Impingement Syndrome.
Study Start Date :
Jun 1, 2014
Actual Primary Completion Date :
Aug 1, 2015
Actual Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Subacromial Impingement Syndrome

Subjects between 18 to 45 years, with Subacromial Impingement Syndrome at least one week.

Procedure: physical therapy
A 20 minutes ice pack cryotherapy applied for 4 consecutive days

Other: ice pack

No Intervention: Control

Healthy subjects between 18 to 45 years.

Outcome Measures

Primary Outcome Measures

  1. Cytokines serum levels [up to 96 hours post cryotherapy]

Secondary Outcome Measures

  1. Pressure pain threshold [72 hours pre cryotherapy and 96 hours post cryotherapy]

  2. Disabilities of the Arm, Shoulder and Hand - DASH questionnaires [72 hours pre cryotherapy and 96 hours post cryotherapy]

  3. Western Ontario Rotator Cuff Index - WORC questionnaires [72 hours pre cryotherapy and 96 hours post cryotherapy]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Definition: The participants will be selected from population in general and will be screened by the inclusion and exclusion criteria below:

Inclusion Criteria:
  • The diagnosis for SIS will be based on a clinical examination and self-reported orthopaedic history. at least 3 positive tests of: Neer impingement test, Hawkins impingement test, Jobe test, Speed test or Gerber test, pain with passive or isometric resisted shoulder lateral rotation, pain with active shoulder elevation and pain with palpation of rotator cuff tendons.
Exclusion Criteria:
  • Fracture, osteoporosis, malignancy, infection, and active inflammatory process, pregnancy, systemic illnesses, physical therapy or manual therapy treatment within 6 months prior to the evaluation, signs of complete rotator cuff tear or acute inflammation, cervicothoracic spine-related symptoms (positive cervical compression test and excessive kyphosis), scoliosis, glenohumeral instability (positive apprehension, anterior drawer, or sulcus tests), or previous upper extremity fracture or shoulder surgery.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UFSCar Physical therapy Department São Carlos São Paulo Brazil 13.565-905

Sponsors and Collaborators

  • Universidade Federal de Sao Carlos
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

Investigators

  • Study Director: Tania Fatima Salvini, Professor, Universidade Federal de Sao Carlos

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Aristides Leite Siqueira Junior, Master Student, Universidade Federal de Sao Carlos
ClinicalTrials.gov Identifier:
NCT02351986
Other Study ID Numbers:
  • U1111-1162-2746
First Posted:
Jan 30, 2015
Last Update Posted:
Mar 22, 2016
Last Verified:
Mar 1, 2016
Keywords provided by Aristides Leite Siqueira Junior, Master Student, Universidade Federal de Sao Carlos
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2016