Flexor tendon injury in zone 1and 2. Spontaneous rupture of flexor tendons
Conditions
Interventions
Intervention 1: Intervention group: The clients will be referred to the occupational therapist within 24-24 hours after surgery. In this group, regular rehabilitation programs and the Strickland proto
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
12 Years to No maximum
Inclusion criteria
Inclusion criteria: Sharp tendon injuries Time lapse 4-2 days after surgery restoration of flexor tendon in Zone 1 and 2 Age 12 years old Not having injuries (fracture in the same limb, extensor tendon damage on the same finger) Not having psychological problems (problems that cause not cooperating with the implementation of therapeutic protocols) Having an acceptable level of cognitive performance, 21 or higher, in the Mini Mental Status Examination (MMSE) The initial repair of the tendon without the need for a transfer or graft tendon Not having a neurological disease (stroke, dementia, Parkinson, etc.) and orthopedic (arthritis and ...) Similar restoration method
Exclusion criteria
Exclusion criteria: Unwillingness to continue cooperation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Score of hand function in Michigan hand outcomes questionnaire (MHQ). Timepoint: Measure hand function at the beginning of the study (before the intervention), 8 weeks after intervention and after follow up (4 weeks). Method of measurement: Michigan hand outcomes questionnaire (MHQ) to measure the hand function.;Satisfaction in activity of daily living in the Canadian Occupational Performance Measure. Timepoint: Measuring satisfaction degree in activity of daily living at the beginning of the study (before the intervention), 8 weeks after the intervention and after follow up (4 weeks). Method of measurement: Canadian Occupational Performance Measure Inventory to measure satisfaction in activity of daily living. | — |
Secondary
| Measure | Time frame |
|---|---|
| Scale of range of motion from goniometer. Timepoint: Measuring the range of motion at the beginning of the study (before the intervention), 8 weeks after the start of the intervention and after the follow up (4 weeks). Method of measurement: Goniometer to measure the range of motion.;Score the pain of the scale of the Visual Analogue Scale. Timepoint: Pain measurements at the beginning of the study (before the intervention), 8 weeks after the start of the intervention and after the follow up (4 weeks). Method of measurement: Visual Analogue Scale to measure pain.;Disability Score in the Disability of the Arm, Shoulder and Hand Questionnaire. Timepoint: Measurement of disability at the beginning of the study (before the intervention), 8 weeks after the start of the intervention and after the follow-up period (4 weeks). Method of measurement: Questionnaire for disability of the arm, shoulder and hand outcome questionnaire to measure disability.;Scale of gross motor performance in Box and Blocks test. Timepoint: Measurement of gross motor function 8 weeks after the start of the intervention and after the follow-up period (4 weeks). Method of measurement: Box and Blocks test to measure gross motor performance.;Fine motor performance score in Purdue Pegboard Test. Timepoint: Measurement of fine motor function 8 weeks after the start of the intervention and after the follow-up period (4 weeks). Method of measurement: Purdue pegboard test to measure fine motor performance.;Score of grasp power from dynamometer. Timepoint: Measuring the grasp power 8 weeks after the start of the intervention and after the follow-up period (4 weeks). Method of measurement: Dynamometer to measure grasp power.;Score of Power pinch of pinch gauge. Timepoint: Measure the power of the pinch 8 weeks after the start of the intervention and after the follow up (4 weeks). Method of measurement: Pinch gauge to measure pinch power. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLaleh Lajevardi
Iran University of Medical Sciences
Outcome results
None listed