Mechanisms of Neurodynamic Treatments (MONET)

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

INTRODUCTION: Carpal tunnel syndrome (CTS) is a relatively common condition caused by compression of one of the main nerves at the wrist, the median nerve. Non-surgical treatments, like steroid injections and physiotherapy, are the first line of treatment for patients with carpal tunnel syndrome. The investigators have previously shown that specific physiotherapeutic exercises (neurodynamic exercises) can reduce the need for carpal tunnel surgery in some patients. Experimental studies in animal models demonstrate that these exercises have an anti-inflammatory effect and can help the nerve to regenerate. However, the exact mechanisms of action of these exercises are not well understood in patients. A better understanding of the mechanisms of action of physiotherapeutic exercises would help clinicians to better target these treatments to those patients who may benefit from them. AIM: To investigate the mechanisms of action of 6 weeks' neurodynamic treatments on nerve function and structure as well as patient-reported outcome measures in patients with CTS compared to a positive control intervention (routine care steroid injection) and a negative control intervention (advice). METHODS AND ANALYSIS: In this single-blind randomised mechanistic trial, patients with confirmed mild to moderate CTS (n=78) and age and gender-matched healthy controls (n=30) will be included. Patients will be randomly allocated to a 6-week neurodynamic exercise group, steroid injection, or advice group. Outcome measures will be explored at baseline (patients and controls), post-intervention (patients), and 6-month follow-up (patients). Outcomes include diffusion-weighted and anatomical MRI of the median nerve at the wrist, quantitative sensory testing, nerve conduction studies, inflammatory markers in blood and skin biopsies, and validated questionnaires for pain, function, and psychological factors. Two-way repeated measures ANCOVAs (factors time and intervention, adjusted for baseline measurements as a continuous covariate) will be performed to identify differences in MRI parameters, clinical assessment, and inflammatory markers between patients in different groups and healthy controls.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

‣ Patients:

• Patients who have a diagnosis of mild to moderate carpal tunnel syndrome based on a clinical assessment and confirmed with nerve conduction studies.

• Male or Female, aged 18 years or above.

• Patient is willing and able to give informed consent for participation in the study.

‣ Healthy participants:

• Male or female aged 18 years or above.

• Participant is willing and able to give informed consent for participation in the study.

• No history of hand or arm symptoms

• No history of neck pain in the past 3 months

• No systemic medical condition

• No strong anticoagulant medication or altered coagulation (e.g., hemophilia) preventing skin biopsies

• Severe anxiety or depression

• Participants are required to be age- \& sex-matched to patient participants

• No contraindications for magnetic resonance scanning at 3T

⁃ Sufficient command of the English language

Locations
Other Locations
United Kingdom
Nuffield Department of Clinical Neurosciences, University of Oxford
RECRUITING
Oxford
Contact Information
Primary
Annina Schmid, PhD
annina.schmid@ndcn.ox.ac.uk
+44 (0) 1865 223254
Backup
Eva Sierra-Silvestre, PhD
eva.sierra@ndcn.ox.ac.uk
+44 (0) 1865 234821
Time Frame
Start Date: 2023-05-17
Estimated Completion Date: 2026-04-01
Participants
Target number of participants: 108
Treatments
Experimental: Neurodynamic exercises
6-weeks home exercise programme of nerve and tendon gliding exercises
Active_comparator: Steroid injection Steroid injection (Depomedrone 40mg)
Single steroid injection into Carpal Tunnel (positive control group)
Other: Advice
The advice group will receive advice but no additional intervention during the 6 week intervention period (negative control group)
Sponsors
Collaborators: Wellcome Trust
Leads: University of Oxford

This content was sourced from clinicaltrials.gov