Effects of Home-based Surface Electrical Stimulation for Patients with Cervical Myofascial Pain Syndrome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-60
SponsorTaipei Medical University WanFang Hospital

About this trial

The aim of this study is to compare the developed home-based surface electrical stimulation program to the controls in computer office workers with MPS.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Time of using computer > 4hrs/day

Neck pain > 2 months

Diagnosis of cervical myofascial pain syndrome

VAS pain ≥ 3 (0~10)

Disqualifiers

Had a history of neck surgery

Pregnancy

Systematic disease (e.g. autoimmune disorders, arthritis, infection, etc.)

Malignancy

Trial design

Design model

Parallel

Treatments tested in this trial

  • Surface electrical stimulation (SES)

    Device

    Participants will undergo 3 weeks (20 minutes/ time, three times/ week) of SES intervention.

  • Remote medical support

    Other intervention

    The remote medical support includes a session of video call with a rehabilitation doctor in the first week and weekly telehealth visits with a live physical therapist or physician. The contents of the video calls contain patient education, stretching exercises teaching and instructions of using SES for MPS.

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: SES combined with telemedical supportExperimental treatment 2 interventions
Group B: SESActive comparator 1 intervention
Group C: No interventionNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Pain intensity

A visual analog scale (VAS, scoring from 0-10) is used to measure a participant's pain intensity. The participant indicates their level of pain on average over the past 3 days.

Time frame
4 weeks

Secondary outcomes

1

Pain intensity

A visual analog scale (VAS, scoring from 0-10) is used to measure a participant's pain intensity. The participant indicates their level of pain on average and at its worst during work or at rest over the past 3 days.

Time frame
8 weeks
2

Range of motion of the neck

The range of motion of the neck is measured by using motion capture system with the IMU (inertial measurement unit) sensors.

Time frame
8 weeks
3

Pain pressure threshold (kg/m2)

The pain pressure threshold is measured by using a hand-held dynamometer.

Time frame
8 weeks
4

Neck disability index (NDI, 0~100%)

The NDI is a questionnaire used for assessing self-rated disability in patient participant with neck pain of mechanical origin.

Time frame
8 weeks

Other outcomes

Sponsors and contacts

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