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Determining the effect of dry needling combination with counterforce brace on lateral epicondylitis

Determining the effect of dry needling combination with counterforce brace on pain, grip strength, and upper limb function in individuals with lateral epicondylitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250224064842N1
Enrollment
39
Registered
2025-04-30
Start date
2025-06-05
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Lateral epicondylitis (Tennis elbow). Lateral epicondylitis

Interventions

Intervention 1: First intervention group: Control group: treatment in group 1 (routine physiotherapy) is performed in a way that includes stretching exercises of the wrist extensor muscles for 30 seco

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: People whose dominant hand is involved No contraindications for using dry needles Pain on palpation of the external epicondyle of the humerus in the dominant hand Cozen's test is positive They have not responded to conservative treatment in the past 6 months No history of corticosteroid injections in the past 6 months

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before the intervention and after the intervention and one month later. Method of measurement: Visual Analogue Scale.;Grip strength. Timepoint: Before the intervention and after the intervention and one month later. Method of measurement: Dynamometer.;Upper limb function. Timepoint: Before the intervention and after the intervention and one month later. Method of measurement: Quick Dash questionnaire.;Pressure pain threshold. Timepoint: Before the intervention and after the intervention and one month later. Method of measurement: Algometer.;Quality of life. Timepoint: Before the intervention and after the intervention and one month later. Method of measurement: 36-question quality of life questionnaire (SF-36).

Secondary

MeasureTime frame
Severity of disability. Timepoint: Before the intervention and after the intervention and one month later. Method of measurement: Patient-Rated Tennis Elbow Evaluation Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh jafari

Shahid Beheshti University of Medical Sciences

razieh.jafari401@gmail.com+98 21 7787 9719

Outcome results

None listed

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