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The Effect of Proprioceptive Neuromuscular Facilitation and Mirror Therapy on Range of Motion, Pain, Functionality, Kinesophobia and Quality of Life in Patients With Upper Extremity Burns

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03997942
Recruitment Status : Recruiting
First Posted : June 25, 2019
Last Update Posted : June 25, 2019
Sponsor:
Information provided by (Responsible Party):
Mine Seyyah, Dr. Lutfi Kirdar Kartal Training and Research Hospital

Brief Summary:
Purpose of the study; The aim of this study was to investigate the effect of two different exercise programs on joint patency, pain, functionality, kinesophobia and quality of life in upper extremity burn patients. Lütfi Kırdar Training and Research Hospital Burn and Wound Center and unilateral upper extremity burns will consist of individuals aged 18-65 years. 48 burn patients who volunteered to participate in the study will be included in the study. Demographic information of the cases will be recorded. Joint range of motion and pain will be evaluated with the Visual Analogue Scale (VAS) before and after the treatment program. Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire will be used to evaluate upper extremity functions. TAMPA Kinezophobia questionnaire will also be used for kinesiophobia. To evaluate the quality of life, Burn-Specific Health Scale developed for burn patients will be used.

Condition or disease Intervention/treatment
Burn; Arm Other: Effect of exercise

Detailed Description:
Joint range of motion of the subjects will be measured with a goniometer. Pain will be evaluated with the Visual Analogue Scale (VAS). In order to evaluate the upper extremity functions, the validity and reliability of the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire, conducted by Tülin Düger et al. The TAMPA Kinezophobia questionnaire, which has been validated and validated in 2011, will be used for kinesiophobia. The Burn-Specific Health Scale developed for burn patients will be used to evaluate the quality of life. The validity and reliability study of the questionnaire was conducted by Mehmet Adam et al.

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Study Type : Observational [Patient Registry]
Estimated Enrollment : 48 participants
Observational Model: Case-Control
Time Perspective: Prospective
Target Follow-Up Duration: 6 Months
Official Title: The Effect of Proprioceptive Neuromuscular Facilitation and Mirror Therapy on Range of Motion, Pain, Functionality, Kinesophobia and Quality of Life in Patients With Upper Extremity Burns
Actual Study Start Date : May 1, 2019
Estimated Primary Completion Date : September 20, 2019
Estimated Study Completion Date : December 15, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Burns

Group/Cohort Intervention/treatment
proprioceptive neuromuscular facilitation
PNF will be applied to randomly selected patients.
Other: Effect of exercise
Once the data are available, we hope to have information about which of the exercise practices included in the rehabilitation program of acute upper extremity burn patients is more effective.

Mirror therapy
Mirror therapy will be applied to randomly selected patients.
Other: Effect of exercise
Once the data are available, we hope to have information about which of the exercise practices included in the rehabilitation program of acute upper extremity burn patients is more effective.

Standart therapy
Standard treatment will be applied to randomly selected patients.
Other: Effect of exercise
Once the data are available, we hope to have information about which of the exercise practices included in the rehabilitation program of acute upper extremity burn patients is more effective.




Primary Outcome Measures :
  1. Demographic information [ Time Frame: 10 minutes ]
    Demographic information of the cases will be recorded.Age, cause of burn, burn zone, burn percentage will be recorded.

  2. Joint range of motion [ Time Frame: 15 minutes ]
    The goniometer will measure the range of motion.

  3. Pain assesment [ Time Frame: 5 minutes ]
    Pain will be assessed by visual pain scale.

  4. Functional assesment [ Time Frame: 15 minutes ]
    Shoulder-Arm Function Questionnaire will be used to evaluate upper extremity functions.

  5. Fear of Motion [ Time Frame: 10 minutes ]
    The Tampa Kinesophobia Questionnaire will be used to assess fear of movement.

  6. Quality of Life Assesment [ Time Frame: 15 minutes ]
    A scale specific to burn patients will be used to evaluate the quality of life.(Burn Specific Health Scale)



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Acute Burn Patients
Criteria

Inclusion Criteria: -18-65 years of age, -the unilateral upper extremity burn, -the understanding of the given information, the application of mirror therapy and the ability to accurately express the level of pain that prevents cognitive, affective and verbal communication There is no problem and no visual impairment, - Turkish reading and writing, - Paralysis, plaster, etc. that will prevent movement in the extremity opposite the burned extremity. to be cognitive enough to understand the surveys,

- Agreeing to participate voluntarily in the study -

Exclusion Criteria:

  • T.C. Ministry of Health Kartal Lütfi Kırdar Training and Research Hospital Burn and Wound Center treated patients between the ages of 0-18,
  • Burn patients who refused to participate in the study, - Patients with bilateral upper extremity burns

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03997942


Contacts
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Contact: Mine Seyyah, Msc 0905333566908 mine-fzt@hotmail.com

Locations
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Turkey
Wound and Burn Center Recruiting
Istanbul, Turkey, 34865
Contact: Mine Seyyah, Msc    0905333566908    mine-fzt@hotmail.com   
Sponsors and Collaborators
Dr. Lutfi Kirdar Kartal Training and Research Hospital
Investigators
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Study Chair: Mine Seyyah DrLutfiKirdar
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Responsible Party: Mine Seyyah, Msc Physiotherapist, Dr. Lutfi Kirdar Kartal Training and Research Hospital
ClinicalTrials.gov Identifier: NCT03997942    
Other Study ID Numbers: Kartal Wound and Burn Center
First Posted: June 25, 2019    Key Record Dates
Last Update Posted: June 25, 2019
Last Verified: June 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Mine Seyyah, Dr. Lutfi Kirdar Kartal Training and Research Hospital:
burn, physiotherapy
Additional relevant MeSH terms:
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Burns
Wounds and Injuries