Effectiveness of Structured Myofacial Chain Exercises After Distal Radius Fracture
Investigation of the Effectiveness of Structured Myofacial Chain Exercise Training Applied in the Early Period After Distal Radius Fracture
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey, 34000
- Bahcesehir university
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being between the ages of 18-70
- Being able to establish written and verbal communication in Turkish
- Post-Op rehabilitation after primary DRF surgery, at 4 weeks, post op at 6 weeks at the l latest
- Fixation using volar plating and nailing method
- Post-op, if instruments were left temporarily, these instruments should be removed before the study
- No previous history of surgery involving the upper extremity
- To have sufficient technological device usage skills and fast internet infrastructure to use video communication technologies without any problems
- Having a device that provides the necessary equipment for video calling
- Having a table and 6 m2 of space to allow exercise in the living area
Exclusion Criteria:
- Occurrence of one of the complex regional pain syndrome subtypes after fracture
- History of any chronic systemic, rheumatological, neurological, vascular disease
- History of traumatic injury to intact extremities and trunk in the last 6 months
- Presence of pain complaints including spine and shoulder pain over 3 according to the Visual Analogue Scale
- Those who use anti-inflammatory drugs
- Presence of cognitive or psychological illness that will prevent cooperation
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
No Intervention: Control Group
Participants will do any exercises.
They will join only assessment sessions.
|
|
|
Active Comparator: Upper Extremity Exercises Group
Participants will treated exercises with focused on upper extremity especially wrist muscles.
|
Participants who have inclusion criterias after DRF reconstrontion pos-op 4. week will included this study.
Certified Physiotherapist who have master of science degree and doctorate student will assessed them before and after treatment with face to face.
Also exercise education will give face to face with same therapist.
After that first sessions patients will progress their standardize or structered exercises pragram with telerehabilition during 4 weeks and 16 sessions.
All sessions will be supervised with physiotherapist.
End of study assessments will perform again with same therapist.
|
|
Experimental: Myofascial Chains Exercises Group
Participants will treated exercises with focused on whole body especilly myofascial chains.
|
Participants who have inclusion criterias after DRF reconstrontion pos-op 4. week will included this study.
Certified Physiotherapist who have master of science degree and doctorate student will assessed them before and after treatment with face to face.
Also exercise education will give face to face with same therapist.
After that first sessions patients will progress their standardize or structered exercises pragram with telerehabilition during 4 weeks and 16 sessions.
All sessions will be supervised with physiotherapist.
End of study assessments will perform again with same therapist.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quick DASH (The Disabilities of the Arm, Shoulder and Hand)
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
Quick-DASH is an 11-item questionnaire that questions a person's limitations in upper extremity problems.
|
Pre treatment and end of study (4 weeks after from first assessment)
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Visual Analogue Scale (VAS)
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
This scale scores from 0 to 10. Higher scores indicate worse pain.
|
Pre treatment and end of study (4 weeks after from first assessment)
|
|
Hand Functional Index (HFI)
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
The hand functional index scale consists of 9 items.
Each item is scored between 0-3.
It is calculated by adding the scores from all items separately for both hands.
|
Pre treatment and end of study (4 weeks after from first assessment)
|
|
Michigan Hand Outcomes Questionnaire (MHQ)
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
It is a survey that includes six subheadings from patients (pain, hand function, satisfaction with hand function, work performance, ADL and aesthetic satisfaction).
|
Pre treatment and end of study (4 weeks after from first assessment)
|
|
Joint Range of Motion Measurement Test With Goniometer
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
Joint range of motion evaluation was made with a goniometer device and flexion, extension, radial-ulnar deviation angles were evaluated.
|
Pre treatment and end of study (4 weeks after from first assessment)
|
|
Hand Grip Strength Measurement Test With Hand Dynamometer
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
During the test, the patient was in a sitting position and the force value was recorded by squeezing the device in the palm of the hand and not supporting the body with the elbow.
|
Pre treatment and end of study (4 weeks after from first assessment)
|
|
Pinch Grip Strength With Pinch Meter
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
The force value was recorded by the researcher, by holding the device from the indicator part and asking the subject to squeeze it between the thumb and index finger in a sitting position.
|
Pre treatment and end of study (4 weeks after from first assessment)
|
|
Fingertip Dexterity and Gross Movement of the Hand With The Purdue Pegboard Test (PPT)
Time Frame: Pre treatment and end of study (4 weeks after from first assessment)
|
With materials such as metal pipe beads and sequin beads inside the device; The subject was asked to perform the exercises against the clock in the order and ways specified in the guide.
|
Pre treatment and end of study (4 weeks after from first assessment)
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- BAU-ALKAN-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Distal Radius Fractures
-
NCT03716661CompletedDistal Radius Fracture | Radius Fracture Distal | Radius Distal Fracture
-
NCT06913933RecruitingDistal Radius Fractures
-
NCT06343467CompletedDistal Radius Fractures
-
NCT07054463Recruiting
-
NCT06617780RecruitingDistal Radius Fractures
-
NCT06255106CompletedDistal Radius Fractures
-
NCT06913894Recruiting
-
NCT06235957Not yet recruitingFractures, Bone | Distal Radius Fractures
-
NCT06299228RecruitingDistal Radius Fractures
Clinical Trials on Therapeutic Exercises
-
NCT04793763Recruiting
-
NCT04322864CompletedMusculoskeletal Diseases | Shoulder Pain
-
NCT04437524Completed
-
NCT04297696CompletedHemophilic Arthropathy
-
NCT06358560Recruiting
-
NCT05521165Not yet recruitingGluteus Medius, Ultrasonography, NSCLBP
-
NCT05855681CompletedKnee Osteoarthritis
-
NCT05321537Completed
-
NCT04205188Completed
-
NCT01314196CompletedShoulder Impingement Syndrome