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Manual and instrumental therapy for the treatment of women's neck pain

Ischemic Compression in the Treatment of Myofascial Pain Syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2q24nb
Enrollment
Unknown
Registered
2019-09-29
Start date
2019-09-10
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Myofascial Pain Syndrome

Interventions

Ischemic Compression Manual: A single session of ischemic compression performed with the physiotherapist's thumb over the trigger point of the upper trapezius muscle, lasting 90 seconds. 16 volunteers
Procedure/surgery
E02.190.599

Sponsors

Universidade Federal de Santa Catarina- UFSC
Lead Sponsor
Universidade Federal de Santa Catarina- UFSC
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Present active trigger point in the upper trapezzius;present pain in the cervical region beginning within three months; present pain level greater than 3 in the visual analogue scale (VAS).

Exclusion criteria

Exclusion criteria: Present whiplash injury and / or cervical pathologies such as disc herniation or Thoracic Gorge Syndrome; be performing treatment for pain in the region of the neck and shoulders; make use analgesics, anti-inflammatory and / or muscle relaxant.

Design outcomes

Primary

MeasureTime frame
Primary outcome - Pain improvement, assessed by visual analog scale (VAS). Data collected before the intervention, 10 min, 30 min, 1 week and 1 month after the intervention.

Secondary

MeasureTime frame
Secondary outcome - increase in pressure pain threshold, assessed by pressure algometry. Data collected before and after 30 min of the intervention. Secondary outcome - Neck disability index, assessed by the neck disability index questionnaire. Data collected before the intervention, 1 week and 1 month after. Secondary outcome - reduction in electromyographic muscle activity assessed by surface electromyography. Data collected before the intervention and 30 min after

Countries

Brazil

Contacts

Public ContactVivian Florianovicz

Universidade Federal de Santa Catarina- UFSC

vflorianovicz@gmail.com+55-54-991552261

Outcome results

None listed

Source: REBEC (via WHO ICTRP)