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The effects of addition of transcranial direct current stimulation to exercise in patients with lateral elbow pain

The effects of addition of transcranial direct current stimulation to therapeutic exercise on pain, functional disability and grip strength in patients with tennis elbow

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140408017177N2
Enrollment
40
Registered
2023-01-01
Start date
2023-01-25
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Tennis elbow. Lateral epicondylitis

Interventions

Intervention 1: active transcranial direct current stimulation group: 1) progressive eccentric exercises of the wrist extensors / 3 sets of 10 repetitions. 2) Extensor carpi radialis brevis muscle str

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 55 Years

Inclusion criteria

Inclusion criteria: unilateral lateral elbow pain for 6 weeks to 1 year average pain intensity of 3 or more on visual analog scale during the last week age between 30 to 55 years a score of 33 or more on the patient-rated tennis elbow evaluation questionnaire pain over the lateral humeral epicondyle provoked by at least two of the following four tests:1) palpation of the external epicondyle, 2) Resisted wrist extension (Thomsen/Cozen's test), 3) Resistance extension of fingers (Maudsley test), 4) Passive stretching of the extensor muscle group (Mills test)

Exclusion criteria

Exclusion criteria: history of local trauma, surgery, physiotherapy treatment or corticosteroid injection in the lateral epicondyle within the last 3 month cervical radiculopathy systemic diseases such as diabetes and rheumatological disorders heart problems history of stroke intracranial surgery, migraine, brain cancer, mental or neurological disorder taking drugs that alter neuronal activity any metal implants, including intracranial electrodes, surgical clips, cochlear implants or pacemakers, or other implanted electronic devices pregnancy or breastfeeding balance disorder or dizziness active infection or scalp or skin condition (e.g., psoriasis or eczema) a head injury that resulted in a loss of consciousness that required further investigation (e.g., a brain scan) seizure epilepsy or a history of epilepsy adverse effects to previous transcranial direct current stimulation or other brain stimulation techniques Covid-19 infection during the study or during one month before the start of the study carpal tunnel syndrome fibromyalgia

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: pre-intervention, post-intervention, 4 weeks post-intervention. Method of measurement: Visual analog scale.;Functional disability. Timepoint: pre-intervention, post-intervention, 4 weeks post-intervention. Method of measurement: Patient-rated tennis elbow evaluation.;Grip strength. Timepoint: pre-intervention, post-intervention, 4 weeks post-intervention. Method of measurement: manual dynamometer.

Secondary

MeasureTime frame
Finger & hand dexterity. Timepoint: pre-intervention, post-intervention, 4 weeks post-intervention. Method of measurement: Perdue pegboard.;Quality of life. Timepoint: pre-intervention, post-intervention, 4 weeks post-intervention. Method of measurement: 12-Item Short Form Survey.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactIman Rezaei

Shiraz University of Medical Sciences

irezaei@sums.ac.ir+98 71 3627 1551

Outcome results

None listed

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