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The Effect of Experimental Neck Pain in Healthy Participants

A

Aalborg University

Status

Unknown

Conditions

Healthy
Neck Pain

Treatments

Other: Injection of Isotonic saline
Other: Injection of NGF

Study type

Interventional

Funder types

Other

Identifiers

NCT03848247
N-20180063_Sub-project_1

Details and patient eligibility

About

This study investigates if/how an experimentally applied muscle pain/soreness, lasting for some days may affect brain activity, balance, movement patterns, muscle function and pain sensitivity in a healthy population

Full description

All included healthy volunteers will participate in test-sessions on 4 separate days over approximately 2 weeks.

During the study participants will be randomised into and either a control group (injection of isotonic saline into a neck muscle) or neck pain group (injection of Nerve Growth Factor (NGF) into a neck muscle).

Alle participants tested with regards to:

Brain activity related to neck muscles will be estimated using TMS Balance will be tested using a force place Body movements will be recorded using 3D tracking Muscle activity will be estimated using electromyography (EMG)

Enrollment

40 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy men and women aged 18-50 years
  • Only for sub-projects 1 and 2: Right-handed
  • Able to speak, read and understand Danish and English

Exclusion criteria

  • Pain from the neck or shoulder area during the past 6 months
  • Experience of delayed onset muscle soreness (DOMS) during the week leading up to the test session
  • Former surgery in neck or shoulder
  • Current or previous chronic or recurrent pain condition
  • Pregnancy
  • Drug addiction defined as the use of cannabis, opioids or other drugs
  • Previous neurologic, musculoskeletal or mental illnesses
  • Regular use of analgesics
  • Abnormally disrupted sleep in the last 24 hours preceding the experiment
  • Lack of ability to cooperate
  • Unable to pass the TASS safety screening questionnaire for TMS

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

40 participants in 2 patient groups

Control group
Experimental group
Description:
Participants will be injected with 0.5ml Isotonic saline into a neck muscle
Treatment:
Other: Injection of Isotonic saline
Neck pain
Experimental group
Description:
Participants will be injected with 0.5ml NGF into the a neck muscle
Treatment:
Other: Injection of NGF

Trial contacts and locations

1

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Central trial contact

Steffan W Christensen, PhD

Data sourced from clinicaltrials.gov

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