Actively Recruiting

Age: 40Years +
All Genders
Healthy Volunteers
ID07281651

Investigating the Role of Central Pain Hypersensitivity in Skeletal Muscle Neural Drive, in People With Knee Pain, and in People With Fibromyalgia Syndrome (Pain-Neural Drive)

Led by University of Nottingham · Updated on 2025-12-15

135

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the role of central pain hypersensitivity and its impact on nerve signaling to skeletal muscles in adults aged 40 years or older. The focus is on people with chronic knee pain, fibromyalgia, and healthy volunteers without chronic pain. The study aims to understand whether changes in nerve signaling relate to physical function and disability in these groups. The study involves two visits to a medical research facility. During the first visit, participants undergo screening, provide consent, and complete questionnaires along with familiarization exercises. The second visit includes detailed sensory testing, muscle electrical activity measurements using electrodes during static muscle contractions, and physical performance tests. A temporary pain stimulus will also be applied during muscle testing to assess its influence on neuromuscular function. Participants will complete questionnaires on pain severity, disability, fatigue, and physical activity. Physical tests include walking, rising from a chair, and balancing. Researchers will measure pain thresholds, muscle motor unit firing characteristics, and physical performance at baseline. The total involvement includes two visits with assessments of pain sensitivity, neuromuscular control, and physical function to explore how chronic pain affects muscle nerve signaling and mobility.

CONDITIONS

Brief Title

Investigating the Role of Central Pain Hypersensitivity in Skeletal Muscle Neural Drive

Who Can Participate

Age: 40Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 40 years or older
  • For knee pain group: history of knee pain with intensity of 4 or higher out of 10 for most days in the past 3 months
  • For fibromyalgia group: previous clinical diagnosis of fibromyalgia and pain intensity of 4 or higher out of 10 for most days in the past 3 months
  • For control group: pain-free individuals without known osteoarthritis
Not Eligible

You will not qualify if you...

  • Body mass index greater than 35
  • Body weight of 250 kg or higher
  • Pregnancy (for women)
  • Unable to give consent
  • Unable to meet requirements of clinical assessment
  • Performed strenuous exercise in past 24 hours before testing
  • Consumed alcohol on day of testing
  • Consumed caffeine on day of testing

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) where screening, eligibility assessment, and informed consent occur

Diagnostic Evaluation

Duration - Up to 2 visits over a short period

Participants attend study visits to undergo clinical assessments, questionnaires, and neuromuscular testing including pain sensitivity and muscle contraction measurements.

2 visits (in-person) involving clinical knee assessment, muscle testing familiarisation, pain sensitivity testing, and questionnaires

Trial Site Locations

Total: 1 location

1

University of Nottingham Graduate Entry Medicine and Health, Royal Derby Hospital, Uttoxeter Road, Derby

Derby, Derbyshire, United Kingdom, DE22 3DT

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Research Team

B

Ben Lightowler, MSc

S

Stephanie Smith, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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