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NCT06299228 · ClinicalTrials.gov registry record · NA
Is Sensorimotor Training Effective Following a Distal Radius Fracture?
A NA study of Distal Radius Fractures, sponsored by Hand Surgery Associates.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT06299228 is a NA study of Distal Radius Fractures that is actively recruiting participants, run by Hand Surgery Associates. The registered enrollment target is 50 participants, below the 184-participant average among 4 other Distal Radius Fractures trials with a reported enrollment target (73% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06299228, a NA study of Distal Radius Fractures, is actively recruiting participants, sponsored by Hand Surgery Associates.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare the short-term outcomes of individuals who have surgery (volar plate) for a wrist (distal radius) fracture who have routine hand therapy treatment versus routine hand therapy treatment and sensorimotor activities. Individuals who meet inclusion criteria at the facilities collecting data will be invited to participate. If they agree to participate, they will randomly and blindly (via concealed envelopes) be assigned to the control (routine treatment) or the sensorimotor treatment group. Data collection will occur at 3- and 6-weeks post initiation of skilled therapy and will include measurement of joint position sense, function via the Patient Rated Wrist and Hand, pain via the Numeric Pain Rating Scale, and range of motion at the digits and wrist.
Conditions Studied
Interventions
- OTHER Control Group
- OTHER Experimental Group
Study Locations (1)
Pennsylvania
- Hand Surgery Associates - Olyphant
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-04 |
| Est. Completion | 2025-04 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06299228
The ClinicalTrials.gov registry entry for NCT06299228 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 184-participant average among 4 other Distal Radius Fractures trials with a reported enrollment target (73% lower). The listed sponsor is Hand Surgery Associates, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Distal Radius Fractures appearing as the primary indexed condition, and to 2 interventions - of which Control Group is the first listed.
NCT06299228 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT06299228 about?
NCT06299228 is a clinical study titled "Is Sensorimotor Training Effective Following a Distal Radius Fracture?". The purpose of this study is to compare the short-term outcomes of individuals who have surgery (volar plate) for a wrist (distal radius) fracture who have routine hand therapy treatment versus routine hand therapy treatment and sensorimotor activities. Individuals who meet inclusion criteria at the...
What is the current status of trial NCT06299228?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2024-04. Estimated completion is 2025-04.
What conditions does trial NCT06299228 study?
This clinical trial studies the following conditions: Distal Radius Fractures.
What interventions are being tested in trial NCT06299228?
The interventions under investigation include: Control Group (OTHER), Experimental Group (OTHER).
Who is sponsoring clinical trial NCT06299228?
This trial is sponsored by Hand Surgery Associates, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06299228 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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