Pain Clinical Trial
Official title:
Effectiveness of a Global Proprioceptive Training After Wrist Fracture
Verified date | November 2023 |
Source | University of Malaga |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this randomized clinical trial is to compare how a program of proprioceptive exercises for the wrist could influence in pain, functionality and quality of life in people that have suffered a wrist fracture. The main questions it aims to answer are: - Evaluate the effect of a specific proprioceptive program on pain and functionality. - Study the relationship between proprioception deficit and functionality. Intervention will be: - Control group: participants of this group are going to receive only standard rehabilitation program after wrist fracture. - Experimental group: participants of this group are going to receive standard rehabilitation program after distal radius fracture and a specific proprioceptive program. Researchers will compare control and experimental group to see if a implantation of a proprioceptive program for the wrist has benefits on pain, function and quality of life.
Status | Not yet recruiting |
Enrollment | 28 |
Est. completion date | September 1, 2024 |
Est. primary completion date | August 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: - Adult (equal or more than 18 y/o). - Suffering a wrist fracture and have passed immobilization period. - Agree and sign informed consent. Exclusion Criteria: - Not had suffered a wrist fracture, being in the immobilization period or not authorized by his/her orthopedic surgeon to start with rehabilitation. - Suffer any mental, cognitive, neurological or musculoskeletal disorder. - Previous injury or pathology of the upper limb affected. - Previos surgery on the upper limb affected. - Have cervical pathology/impairment. - Suffering from blindness. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Malaga |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in function related with daily living activities | Measured with QuickDASH. 11 items, 0=no disability and 100= total disability | Baseline, 4 weeks and 3 months. | |
Primary | Change in perception of pain, referred to wrist | Pain measured with Numerical Rating Scale (NRS) 0= no pain and 10=worst pain | Baseline, 4 weeks and 3 months | |
Primary | Change in hand and wrist function related with difficulties in performing daily living activities | Measured with Patient-rated wrist evaluation (PRWE). 15 items in 2 subscales, function (10 items) and pain (5 items). Punctuation could be from 0 to 50 in each subscale, where 50 points means worse pain/function. | Baseline, 4 weeks and 3 months | |
Secondary | Change in range of motion of the wrist | Active range of motion of the wrist in all planes of motion. Assessed with a goniometer. | Baseline, 4 weeks and 3 months. | |
Secondary | Change in strength | GRIP force. Assessed with a Jamar Dynamometer. | Baseline, 4 weeks and 3 months. | |
Secondary | Change in Perception of Quality of life | EuroQol-5D. It has 5 dimensions, mobility, self-care, daily activities, pain and anxiety and depression. Patient determines the level of agreement with the affirmations (3 options). | Baseline, 4 weeks and 3 months | |
Secondary | Changes in proprioception, position terms | Measured with Joint Position Sense Test (JPST). | Baseline, 4 weeks and 3 months | |
Secondary | Changes in proprioception, strength terms | Measured with Force Sense Test | Baseline, 4 weeks and 3 months |
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