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Cupping in patients with neck pain.

Effects of cupping therapy on myofascial trigger points in the upper trapezius muscle of patients with chronic neck pain.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-46kbnp
Enrollment
Unknown
Registered
2018-02-26
Start date
2018-04-30
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

Chronic Neck Pain/ Physiotherapy Modalities

Interventions

Cupping group The application of acrylic suction cups with a diameter of 4 cm and volume of 260 mL (Cosmos International Supplies, New Taipei City, Taiwan) will be used. The suction cup will be applie
Other
E02.779

Sponsors

Departamento de Ciências da Saúde e Biológicas da Universidade Federal do Amapá
Lead Sponsor
Departamento de Ciências da Saúde e Biológicas da Universidade Federal do Amapá
Collaborator

Eligibility

Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Neck Disability Index (NDI) score>5 points and punctuation on the Numeric Rating Scale (NRS) > 3; Present bilateral and active trigger point, centrally located in the trapezius muscle descendent fibers.

Exclusion criteria

Exclusion criteria: The exclusion criteria adopted in the present study will be individuals with a history of cervical trauma; head, face or cervical surgery; cervical hernia; degenerative diseases of the spine; have undergone physiotherapeutic treatment in the last three months; use of analgesic, anti-inflammatory or muscle relaxants in the last week; presence of systemic diseases; medical diagnosis of fibromyalgia.

Design outcomes

Primary

MeasureTime frame
Increase in pressure pain threshold, verified through algometry for a variation of at least 5% in pre and post-intervention measurements.

Secondary

MeasureTime frame
Reduction in pain intensity, quantified using the Numerical Pain Scale from a variation of at least 5% in the pre- and post-intervention measurements.;Reduction in cervical disability, assessed by the Neck Disability Index (NDI) questionnaire from a variation of at least 5% at the beginning and at the end of the interventions.; Reduction of catastrophization, quantified through the Pain-Related Self-Statement Scale (PRSS) questionnaire from a variation of at least 5% in the pre- and post-intervention measurements.;Change in cutaneous temperature, assessed by infrared thermography from a variation of at least 5% in pre and post-intervention measurements.

Countries

Brazil

Contacts

Public ContactCleuton Landre

Departamento de Ciências da Saúde e Biológicas da Universidade Federal do Amapá

cleutinho@hotmail.com+55(96)981220910

Outcome results

None listed

Source: REBEC (via WHO ICTRP)