Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT05318729

Use of a Vibration Tool for Postoperative Pain Control in Distal Radius Fractures

The purpose of this research study is to determine if using a vibration tool improves pain control after surgical treatment of distal radius fracture. Additionally, the investigators would like to determine if this tool has any impact on consumption of pain medications postoperatively.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Traditionally, occupational therapists have utilized vibration for sensory re-education in compression neuropathies and peripheral nerve injuries. Vibration is also commonly used for desensitization of hypersensitivity following amputation, crush injury, and for hypersensitive scarring. Since the vibration tool is readily available in the hand therapy clinic, vibration analgesia should be further explored in the hand clinic to help reduce pain. Vibration is a simple, and non-invasive, tool and would be easy, economical, and practical to implement into the hand clinic for postoperative pain control. This research project will evaluate whether vibration can be a useful adjunct to current postoperative pain modalities. With a multidisciplinary approach, the investigators hope to highlight the use of non-opioid modalities of pain control in distal radius fractures and believe that the findings from this study may apply to other painful conditions of the hand as well.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with a distal radius fracture who have undergone an open reduction and internal fixation using a volar FCR approach with a single volar plate
  • Patients who can read, write, and follow direction in English
  • Willing to undergo occupational therapy at Northwestern Medicine's Hand Surgery clinic

Exclusion criteria

  • Patients undergoing oncologic surgery
  • Patients who undergo simultaneous surgery such as open carpal tunnel
  • Patients who only require closed reduction of distal radius fractures
  • Operative patients that require dorsal plate fixation or separate radial styloid plate fixation

Treatment and study plan

Vibration tool

Device

Therapeutic mini massager for scar management, desensitization, muscle stimulation, oral stimulation and sensory re-education. Seek pain relief for sore achy muscles, tendons or bones.

Other names: Norco NC70209 Mini Massager

Primary outcomes

  1. QuickDASH (Disabilities of the Arm, Shoulder, and Hand) Questionnaire

    Time frame: up to 8 week post-surgery

    An 11-item, self-report questionnaire designed to measure physical function and symptoms in patients with any or several musculoskeletal disorders of the upper limb; scored from 0 (no disability) to 100 (most severe disability).

  2. PROMIS Bank v1.1 - Pain Interference Computer Adaptive Test

    Time frame: up to 8 weeks post-surgery

    A 4-6 item self-reported questionnaire designed to measure the consequences of pain on relevant aspects of a person's life; the T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation of 10; low scores represent less pain interference, while high scores represent greater interference.

  3. PROMIS Bank v2.0 - Upper Extremity Computer Adaptive Test

    Time frame: up to 8 weeks post-surgery

    A 4-6 item self-reported questionnaire designed to measure upper extremity function; the T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation of 10; low scores represent less function, while high scores represent greater function.

  4. Pain Visual Analog Scale (VAS)

    Time frame: up to 8 weeks post-surgery

    Scored from 0 (no pain) to 10 (worst possible pain)

Secondary outcomes

  1. Opioid Use

    Time frame: up to 8 weeks post-surgery

    Number of opioid pain medication tablets consumed

Study contacts

Contact information is provided by the study sponsor or research team.

Melissa J Shauver, MPH

CONTACT

[email protected]

312-472-6024

Sadie N Sial, BS

CONTACT

[email protected]

312-695-4463

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Registry information

Official study title

Application of a Unique Vibration Modality for Postoperative Pain Control in Patients With Distal Radius Fractures to Reduce Postoperative Pain and Opioid Use

Important dates

Study start
2027
Primary completion
2028
Study completion
2029
First posted
Apr 8, 2022
Registry last updated
Jul 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.