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Effectiveness of Graded Motor Imagery to Improve Hand Function in Patients With Distal Radius Fracture

Phase 2
Completed
Conditions
Distal Radius Fracture
Pain
Interventions
Procedure: Cognitive Therapy
Registration Number
NCT02838446
Lead Sponsor
Hacettepe University
Brief Summary

The purpose of this study was to investigate of the effectiveness of Graded Motor Imagery (GMI) on hand functionality in patients with Distal Radius Fracture (DRFx). This study was carried out on 36 patients. These patients were randomly assigned to two groups: classic treatment group (n=19) and GMI group (n=17). Both groups received a 8-week (2 days a week) physical therapy and rehabilitation intervention. Outcome measurements were based on upper extremity functional status (Disability of the Arm Shoulder Hand and Michigan Hand Questionnaire scores), pain (on the rest and during the activity with Visual Analog Scale), range of motion (wrist flexion, extension, ulnar/radial deviation, supination and pronation with goniometer), grip strength (standard grip strength with Jamar hydraulic hand dynamometer; lateral, palmar and pinch strength with pinch meter).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria
  • ages between 18-65 years
  • diagnosed with DRFx which is extra-articular
  • managed with pins, internal fixation and/or cast
Exclusion Criteria
  • unwilling or unable to participate
  • intra-articular and instable fractures containing other part of the fractures
  • fractures related with the malignancy and other neurologic diseases
  • existing inflammatory joint condition,
  • lack of cognitive function.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cognitive TherapyCognitive TherapyGraded motor imagery program was applied in only intervention group for 8 weeks.
ControlCognitive TherapyRehabilitation program applied in both groups for 8 weeks. Frequency of the treatment was 2 days in per week and its duration was approximately one hour in one session.
Primary Outcome Measures
NameTimeMethod
Physical Function and Symptoms8 weeks

Disability of the Arm, Shoulder and Hand (DASH) questionnaire scores range from 0 to 100 with a higher score indicating higher degree of disability.

Secondary Outcome Measures
NameTimeMethod
Pain intensity8 weeks

Visual Analog Scale (VAS) is used to evaluate pain intensity. The scale was consisted of a standard line labeled 0 on the left and 10 on the right. (0: no pain, 10: the worst pain).

Normal range of motion8 weeks

Active range of motions of wrist regarding flexion, extension, ulnar deviation, radial deviation, supination and pronation were evaluated with universal goniometer and recorded as degree.

Grip Strength8 weeks

Grip strength was measured in kilograms using a calibrated Jamar Hydraulic Hand Dynamometer with the elbow flexed to 90 degree.

Trial Locations

Locations (1)

Medipol University

🇹🇷

Istanbul, Turkey

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