Skip to content

Cupping therapy for neck pain and disability

Cupping therapy for neck pain and disability

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3578vwr
Enrollment
Unknown
Registered
2023-11-04
Start date
2023-11-06
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

Neck Pain

Interventions

For the Cupping Group (CG): 23 individuals with neck pain will initially receive cupping therapy using the sweeping technique. This involves applying 10ml of grape seed oil for skin hydration, followe
VB21 (Vesícula Biliar, acuponto 21/GB21 (Gallbladder, acupoint 21) (jianjing) e ID14 (Meridiano do Intestino delgado, acuponto 14)/SI14 (Small intestine Meridian, acupoint 14) (jianwaishu) B10/BL10 (t
E02.779

Sponsors

Universidade Federal de Pernambuco
Lead Sponsor
Departamento de Fisioterapia da Universidade Federal de Pernambuco
Collaborator

Eligibility

Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: Visual Analogue Scale (VAS) greater than or equal to 3 points; Neck Disability Index (NDI) greater than or equal to 13 points

Exclusion criteria

Exclusion criteria: Pregnant or lactating women; patients who use anticoagulants; anemia; use of opioid analgesics (examples: Morphine, Tramadol, Hydromorphone, Fentanyl, and others) at the time of data collection or up to three months prior; patients presenting red flags (vertebral fracture, vertebral tumor, vertebral infection; systemic diseases (autoimmune, infectious, vascular insufficiency, renal insufficiency, hepatic insufficiency, neoplasia); fibromyalgia; cervical disc herniation; previous spine surgery; patients with open or poorly healing wounds in the cervical region; cervical brachialgia; alteration of skin integrity and people who have been previously treated with cupping therapy

Design outcomes

Secondary

MeasureTime frame
The expectation is to find a mean difference of at least 12.75 points in the reduction of the level of functional disability in the questionnaire verified by the Neck Disability Index (NDI) in the cupping group compared to the sham group

Primary

MeasureTime frame
It is expected to find a mean difference of at least 2 in pain intensity verified by the Visual Analog Scale (VAS) in the cupping group compared to the sham group.

Countries

Brazil

Contacts

Public ContactThaynara Barreto

Departamento de Fisioterapia da Universidade Federal de Pernambuco

thaynara.barreto@ufpe.br55(81)985611410

Outcome results

None listed

Source: REBEC (via WHO ICTRP)