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Sensory Training in Distal Radius Fractures

I

Istanbul University

Status

Not yet enrolling

Conditions

Distal Radius Fractures

Treatments

Other: Conventional therapy
Other: Sensory Training

Study type

Interventional

Funder types

Other

Identifiers

NCT06894485
IstanbulUr

Details and patient eligibility

About

This randomized controlled trial examines the effectiveness of sensory training in patients undergoing rehabilitation for distal radius fractures. Forty-four participants (aged 18-65, with no prior upper extremity injuries) will be randomly assigned to a control group (conventional physiotherapy) or an experimental group (conventional physiotherapy plus sensory training, including desensitization and proprioception exercises). Assessments will be conducted at baseline, 4 weeks, and 8 weeks using grip strength, sensory function, fine motor skills, pain level, and functional capacity measures. The study aims to compare the impact of sensory training versus conventional physiotherapy on pain reduction, sensory recovery, grip strength, and functional hand use.

Full description

This study aims to investigate the effectiveness of sensory training in patients with distal radius fractures. Designed as a randomized controlled trial, the study will include 44 participants aged 18-65 years who have not had a prior upper extremity injury and are in the rehabilitation phase after a fracture. Participants will be randomly assigned to either the control group (receiving conventional physiotherapy) or the experimental group (receiving conventional physiotherapy plus sensory training, including desensitization and proprioception exercises).

Assessments will be conducted before treatment, at 4 weeks, and at 8 weeks. The evaluation tools will include grip strength (hand dynamometer & pinch meter), sensory function (monofilament test), fine motor skills (Nine-Hole Peg Test - NHPT), pain level (Numerical Pain Rating Scale - NPRS), and functional capacity (DASH questionnaire).

The aim of this study is to compare the effects of sensory training versus conventional physiotherapy on pain reduction, sensory recovery, grip strength, and functional hand use.

Enrollment

44 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18-65 years
  • Diagnosed with distal radius fracture
  • In the rehabilitation phase after fracture healing
  • No prior upper extremity injuries
  • No neurological or psychiatric disorders affecting hand function
  • Able to comply with the rehabilitation program

Exclusion criteria

  • Any other musculoskeletal injury affecting the upper limb
  • Previous upper extremity surgeries
  • Severe neuropathy or sensory disorders
  • Uncontrolled chronic pain conditions

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

44 participants in 2 patient groups

Control
Experimental group
Description:
* Conventional range of motion (ROM) exercises * Muscle strengthening exercises * Fine motor skill exercises * Functional rehabilitation exercises The group will be followed 3 times per week for 8 weeks.
Treatment:
Other: Conventional therapy
Experimental
Experimental group
Description:
* Conventional range of motion (ROM) exercises * Muscle strengthening exercises * Fine motor skill exercises * Functional rehabilitation exercises • Experimental Group: (Conventional therapy + Sensory Training) * Desensitization training (exposure to various textures and stimuli to improve sensory tolerance) * Proprioceptive exercises (closed-eye position sense training, weight transfer exercises) * Tactile stimulation The group will be followed 3 times per week for 8 weeks.
Treatment:
Other: Sensory Training
Other: Conventional therapy

Trial contacts and locations

1

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Central trial contact

TUGBA CIVI KARAASLAN, Asst. Prof. Dr.

Data sourced from clinicaltrials.gov

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