Hand Burn Injury. Burn of unspecified degree of wrist and hand
Conditions
Interventions
Intervention 1: Intervention group: The intervention group received interventional interventions after two weeks (6 sessions) and received conventional interventions such as stretching, exercises for
receiving interventions based on acupuncture The CO-OP protocol is used in this group. Intervention 2: Control group: The control group only received the most common rehabilitation interventions, incl
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 18-65 years old 3-5 days after surgery Having an acceptable level of cognitive performance, score 21 and above, in the Expedient Examination Test (MMSE). Depth of burn 2 and 3, and burn circumference 2.5%. Not having any injuries such as fractures, tendon injuries, or injured infections. Psychological problems that lead to non-cooperation with the implementation of therapeutic protocols
Exclusion criteria
Exclusion criteria: Lack of cooperation and willingness to continue cooperation. Missing more than two sessions. Unwanted side effects after surgery such as infection, severe swelling and recurrence of ulcers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occupational Performance rate in the Canadian Occupational Performance Measure. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: Canadian occupational Performance measure (COPM).;Hand Performance rate in the Michigan Hand Questionnaire. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: Michigan Hand Questionnaire (MHQ).;Disability rate in Shortened Disabilities of the Arm, Shoulder and Hand Questionnaire. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: Shortened Disabilities of the Arm, Shoulder and Hand Questionnaire(Q-DASH). | — |
Secondary
| Measure | Time frame |
|---|---|
| The amount of pain. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: Visual Analog Scale.;Goniometer. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: Goniometer.;Edema rate. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: meter.;Muscle strength. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: Dynamometer.;Ability to perform Activities of Daily Living. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: Modified Barthel Index (MBI).;Quality Of Life level. Timepoint: Time intervals for evaluation at the beginning of the study (before the intervention), after the second week, after the eighth week and after the sixteenth week. Method of measurement: World Health Organization Quality Of Life-Brief (WHOQOL-BRIEF ). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahnoosh Khanipour
Iran University of Medical Sciences
Outcome results
None listed