Evaluation of The Effect of Music Therapy on Fear of Needle Electromyography

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorTC Erciyes University

About this trial

Electroneuromyography (ENMG) is a frequently employed methodology in the diagnosis and monitoring of neuromuscular disorders. It encompasses two principal components: nerve conduction studies (NCS) and needle electromyography (EMG). While NST is conducted with the application of electrical stimulation, which may result in mild discomfort, needle EMG is employed for the examination of muscle electrical activity. It is acknowledged that the procedure may cause discomfort, anxiety and fear in patients, which may have an adverse effect on the test results. A variety of methods have been proposed to mitigate discomfort, including oral ibuprofen, cognitive therapy, and topical agents. Music therapy has demonstrated efficacy in alleviating anxiety and pain during numerous medical procedures; however, its impact on pain and anxiety during needle EMG remains unexplored. This study aims to examine the influence of music therapy on pain and anxiety in individuals undergoing needle EMG. To this end, the effects of needle EMG and music therapy on pain and anxiety will be contrasted in two distinct groups.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 18-70 years referred to the Electroneuromyography Unit with a prediagnosis of lumbosacral radiculopathy

Patients whose cognitive status is sufficient to complete the study and who can be co-operated with

Disqualifiers

Individuals with hearing impairment and/or the use of hearing aids

Patients with a history of significant neurological or psychiatric illness.

Patients with cognitive impairment

Patients with a diagnosis of polyneuropathy.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Music intervention

    Other intervention

    This group will receive music therapy while performing Needle EMG

Treatment groups

58 Participants
are divided into 2 treatment groups
Group A: Control groupNo intervention 0 interventions
Group B: Music GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Visual analogue scale (VAS)

The patient's perception of pain during the procedure will be assessed with the visual analogue scale (VAS) The degree of satisfaction of the patients with the procedure, their willingness to repeat the procedure in the future, the degree of anxiety during the procedure, and the perceived degree of difficulty in the procedure by the physician performing the procedure will be evaluated with VAS between 0 and 10 points.

Time frame
degree of pain during needle EMG, degree of satisfaction with the procedure during needle emg, Whether they are willing to repeat the procedure in the future after needle EMG, anxiety about the procedure: before, during and immediately after procedure
2

State-Trait Anxiety Inventory (STAI)

Time frame
before and immediately after procedure
3

Beck Anxiety Inventory

Time frame
before and immediately after procedure
4

Hospital Anxiety and Depression Scale

Time frame
before and immediately after procedure

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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