Trials / Completed
CompletedNCT01518179
Compression Gloves for Distal Radius Fracture
The Effect of Wearing Made-to-Measure Compression Gloves on Rehabilitation Following DRF.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 35 (actual)
- Sponsor
- Clalit Health Services · Academic / Other
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
Distal Radius Fractures are among the most common orthopedic injuries. Rehabilitation may be characterized by pain, stiffness, swelling, and decreased range of motion (hand and fingers), and grip strength. Compression gloves are used to enhance rehabilitation after various clinical conditions and injuries. However, there are no reports on the effect of compression gloves following Distal Radius Fracture (DRF). This study aims to assess the incremental effect of wearing Made-to-Measure Compression Gloves on rehabilitation following DRF. Working Hypothesis: The addition of Made-to-Measure Compression Gloves to routine follow up and treatment will enhance rehabilitation, when compared with routine follow up and treatment, in patients following Distal Radius Fracture. ICD 10, Version 2010, conditions to be included in the study (defined jointly as Distal Radius Fractures): S52.5 Fracture of lower end of radius (Colles' fracture, Smith's fracture) S52.6 Fracture of lower end of both ulna and radius S52.7 Multiple fractures of forearm Excl.: fractures of both ulna and radius: lower end (S52.6), shafts (S52.4). S52.8 Fracture of other parts of forearm (Lower end of ulna, Head of ulna)
Detailed description
Individuals referred for rehabilitation following DRF will be invited to participate in the study. After obtaining an informed consent individuals will be randomized to receive routine follow up and treatment with or without compression glove. Individuals randomized to made to measure compression gloves will receive them within a week of enrolment. All participating individuals will be assessed by an occupational therapist at enrolment and 2, 4, and 8 week after enrolment. Additional telephone interview, to assess long term effect, will be conducted at 3, 6 and 12 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Made-to-Measure Compression Gloves | Made-to-Measure Compression Gloves in addition to routine follow up and treatment. |
| OTHER | Routine follow up and treatment | Control |
Timeline
- Start date
- 2012-04-01
- Primary completion
- 2018-12-31
- Completion
- 2018-12-31
- First posted
- 2012-01-25
- Last updated
- 2019-01-31
Locations
2 sites across 1 country: Israel
Source: ClinicalTrials.gov record NCT01518179. Inclusion in this directory is not an endorsement.