Radius Fractures
Conditions
Interventions
This is a randomized controlled clinical trial parallel of two arms with an allocation ratio of 1:1 that will include a total of 62 female participants with surgically treated distal radius fracture d
Sponsors
Hospital Herminda Martin
Universidad San Sebastián
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Women; over 18 years old; diagnosed with Unilateral Distal Radius Fracture and treated surgically
Exclusion criteria
Exclusion criteria: Polytraumatized patients; patients with secondary distal radius fractures (tumors, pathological bone, etc.); complicated distal radius fractures (associated with other musculoskeletal, vascular, or neurological injuries); patients with decompensated rheumatic, neurocognitive, or psychiatric diseases; patients with visual impairment preventing completion of study protocols; cognitive impairment assessed with the Mini-Mental State Examination (MMSE); and patients with complex regional pain syndrome (CRPS) at baseline
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to observe a statistically significant improvement in upper limb functionality, measured by the Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) questionnaire, in favor of the experimental group compared with the control group, after the intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to observe a statistically significant reduction in pain intensity, measured using the Numeric Rating Scale (NRS), in favor of the experimental group compared with the control group, after the intervention;A statistically significant decrease in pain interference with daily activities, assessed using the Brief Pain Inventory (BPI), is expected in favor of the experimental group compared with the control group, at the end of the intervention;A significantly lower proportion of cases of complex regional pain syndrome, determined according to the Budapest diagnostic criteria, is expected in the experimental group compared with the control group, at the end of the intervention;A statistically significant improvement in cognitive function, measured by the Abbreviated Mini-Mental Test, is expected in favor of the experimental group compared with the control group, after the intervention;A statistically significant improvement in health-related quality of life, assessed using the EQ-5D-5L questionnaire, is expected in favor of the experimental group compared with the control group, after the intervention | — |
Countries
Chile
Contacts
Public ContactEsteban Vidal Jiménez
Hospital Herminda Martin
Outcome results
None listed