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IRCT20141221020380N3 IRCT 2018-07-14 Kerman University of Medical Sciences Evaluation of a multimedia app for patients with Thoracic Outlet Syndrome and Low Back Pain Evaluation of multimedia mobile application effects on patients with Thoracic Outlet Syndrome and Low Back Pain comparing with control group - a randomized controlled trial 2019-04-01 anticipated 176 Complete https://irct.ir/trial/29974 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: In this study, simple randomization method will be used based on random number table, Blinding description: The participants do not know in which group, intervention or control, will be allocated. The data analyst does not know which patient will be allocated to intervention or control groups. 3 Condition 1: low back pain. Condition 2: thoracic outlet syndrome. Intervention 1: Intervention Group: In the intervention group, the application install on the patient's mobile phone and the patient uses the application for 6 weeks. Intervention 2: Control Group: This group does not install the app and continue normal treatment. No - There is not a plan to make this available Justification or reason for not sharing IPD is To get the required permission from the patient and/or physician
public Saeideh Goharinejad
Kerman, Shariati St., Alley No. 6
Kerman Iran (Islamic Republic of) 7614663454 +98 936 549 2286 gohari.2490@gmail.com Kerman University of Medical Sciences scientific Afshin Sarafi Nejad
Unit 1, First Floor, A-1 Block, Doctors Campus Residential Complex, Doctor Blvd, Kerman
Kerman Iran (Islamic Republic of) 00 +98 34 3261 5849 asarafinejad@kmu.ac.ir Kerman University of Medical Sciences Iran (Islamic Republic of) People's willingness to complete the questionnaire and use the software The patient has an adequate level of cognitive and physical literacy familiar with how the smartphone works. 18 years 65 years Both Patients with any other illness will exclude from the study M54.5 G54.0 Low back pain Brachial plexus disorders Rehabilitation Rehabilitation Intervention Group: In the intervention group, the application install on the patient's mobile phone and the patient uses the application for 6 weeks. Control Group: This group does not install the app and continue normal treatment The Severity of Pain. Timepoint: At the beginning of the study (before the intervention) and 6 weeks after the intervention (use of the application). Method of measurement: Numeric Rating Scale. EAST Test. Timepoint: At the beginning of the study (before the intervention) and 6 weeks after the intervention (use of the application). Method of measurement: By specialist: Record the amount of time a patient can hold his/her hands above the head. Disability of Low Back Pain Patients. Timepoint: At the beginning of the study (before the intervention) and 6 weeks after the intervention (use of the application). Method of measurement: Roland Morris Disability Questionnaire. Thoracic Outlet Syndrome Disability Questionnaire. Timepoint: At the beginning of the study (before the intervention) and 6 weeks after the intervention (use of the application). Method of measurement: Questionnaire. شرکت پژوهشگران داده پرداز ابن سینا حکیم Kerman University of Medical Sciences شرکت پژوهشگران داده پرداز ابن سینا حکیم Approved 2018-04-29 Ethics committee of Kerman University of Medical Sciences Seven Alavi Gardens, Kerman University of Medical Sciences Kerman Kerman Iran (Islamic Republic of)