Effects of Dry Needling Technique in Hip Muscles in Subjects With Grade I-III Hip Osteoarthritis

University of Zaragoza

Status: Unknown

Conditions: Hip Osteoarthritis

Treatments: Other: Sham Dry needling; Other: Dry needling

Study type: Interventional

Funder types: Other

Identifiers

NCT03202056

C.I.PI17/0182

Details and patient eligibility

About

Dry needling is a new treatment technique, addressed to mechanical pain of the neuromusculoskeletal system. Recent investigations has developed new hypothesis about the etiology of the osteoarthritis and could be in relation to musculoskeletal disorders, but there is no published studies evaluating the results of this technique in hip osteoarthritis patients.

The objective of this trial is to evaluate if dry needling is more effective in symptoms, function, range of motion, strength, muscular length, pain threshold and compared to sham dry needling and control.

For this purpose the investigators conduct a randomized controlled trial double-blind (patient and examiner). The investigators included patients diagnosed of hip osteoarthritis Grade I-III by Scale of Kellgren and Lawrence.

Patients included are randomized into 3 groups one receive Dry needling, other sham dry needling and the other is a control. Groups receive 3 treatment sessions.

The variables are measured at the beginning and end of treatment. And also some variables are measured before and after each session. Patients who participated in sham dry needling or control group, when the intervention finish the investigators will be given the opportunity to receive the actual technique.

Enrollment: 45 estimated patients

Sex: All

Ages: 50 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Diagnosed medically with a X-Ray test
• American College of Rheumatology Criteria

Exclusion criteria

• Secondary osteoarthritis by a traumatism, Paget disease, inflammatory or metabolic disease, congenital diseases etc.
• Vascular or neurological disease.
• Musculoskeletal pathologies in lumbar spine, pelvis or lower limbs
• Grade IV in Kellgren and Laurence Scale
• Fear of needles

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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45 participants in 3 patient groups

Dry needling

Experimental group

Description:

Dry needling technique in each active myofascial trigger point once per week for 3 weeks.

Treatment:

Other: Dry needling

Sham Dry needling

Sham Comparator group

Description:

Sham Dry needling technique in each active myofascial trigger point once per week for 3 weeks.

Treatment:

Other: Sham Dry needling

Control

No Intervention group

Description:

Control group. No intervention.