Skip to content

Effectiveness of Biofeedback Therapy compared to Acupuncture for treatment of myofascial pain syndrome in neck and upper back area: A Randomized clinical trial

Effectiveness of Biofeedback Therapy compared to Acupuncture for treatment of myofascial pain syndrome in neck and upper back area: A Randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100127003217N12
Enrollment
50
Registered
2019-02-19
Start date
2019-02-20
Completion date
Unknown
Last updated
2019-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myofacial pain syndrome. Other chronic pain

Interventions

Intervention 1: Intervention group: patients in group A were treated with biofeedback for 6 sessions. Patients, Before and after treatment( immediately and 12 weeks after treatment), were evaluated wi

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Presence of neck and shoulder’s muscles pain for more than 2 months and less than 1 year Presence of at leats 3 trigger points around the neck and shoulder muscles VAS between 4-10 The desire to participate in the study

Exclusion criteria

Exclusion criteria: If there is radiculopathy based on history and the presence of one of radiculopathy’s findings such as weakness , radicular pain, reduced DTR, paresthesia and positive spurling test Presence of confirmed cervical discopathy with MRI Presence of severe cervical degenerative changes History of surgery or cervical spine trauma History of therapeutic intervention for recent neck problems Presence of systemic diseases that prevent acupuncture or biofeedback therapy, such as hemorrhagic, rhomatologic or cardiovascular disorders Patients with history of depression or Taking psychological drugs People with diagnosis of fibromyalgia Pregnancy Malignancy

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before, immediately and 3 months after treatment. Method of measurement: Visual analogue scale ( VAS ).;Neck functional disability. Timepoint: Before, immediately and 3 months after treatment. Method of measurement: Neck disability Index questionare.;Pain pressure treshold. Timepoint: Before, immediately and 3 months after treatment. Method of measurement: Algometer.;Neck range of motion in flexion, extension, left and right lateral bending. Timepoint: Before, immediately and 3 months after treatment. Method of measurement: Bubble inclinometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli pirani

Tabriz University of Medical Sciences

A.pirani90@yahoo.com+98 41 3384 6093

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026