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Effect of Transcutaneous Electrical Nerve Stimulation and Cupping Therapy in The Treatment of Tennis Elbow: A Randomized Controlled Trial

Not Applicable
Completed
Conditions
Tennis Elbow
Interventions
Other: conventional therapy
Device: TENS
Other: cupping therapy
Other: TENS and cupping therapy
Registration Number
NCT04867811
Lead Sponsor
October 6 University
Brief Summary

One hundred and twenty patients (67 females and 53 males) with unilateral TE were included in the study from January 2020 to December 2020 and diagnosed by an orthopedist. Their ages ranged between 20 and 50 years old.

Detailed Description

They were divided randomly into three groups by lottery method. Group A (n=30) received conventional therapy, group B (n=30) received TENS in addition to conventional therapy, group C received cupping therapy with conventional therapy and group D (n=30) received TENS and cupping therapy plus conventional therapy. All patients read and signed a consent form before participation in this trial. This study was approved by the Ethical Committee of the Faculty of Physical Therapy, October 6 University, Egypt. Patients with pain in the lateral epicondylar region, increased pain with pressure and resistance to wrist extension, persistence of symptoms for more than three months, no physical therapy interventions during the last three months were included in the study while patients with bilateral tennis elbow, proximal radio-ulnar joint synovitis, radial nerve entrapment, cervical spine radiculopathy, other diseases like medial epicondylitis, impaired sensibility and paralysis that may affect the outcome measurement and previous injury or surgery in the region of common extensor origin were excluded from this study.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Patients with pain in the lateral epicondylar region, increased pain with pressure and resistance to wrist extension, persistence of symptoms for more than three months, no physical therapy interventions during the last three months
Exclusion Criteria
  • patients with bilateral tennis elbow, proximal radio-ulnar joint synovitis, radial nerve entrapment, cervical spine radiculopathy, other diseases like medial epicondylitis, impaired sensibility and paralysis that may affect the outcome measurement and previous injury or surgery in the region of common extensor origin

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
group Aconventional therapyreceived conventional therapy
group BTENSreceived TENS in addition to conventional therapy
group Bconventional therapyreceived TENS in addition to conventional therapy
group Ccupping therapyreceived cupping therapy with conventional therapy
group Cconventional therapyreceived cupping therapy with conventional therapy
group DTENS and cupping therapyTENS and cupping therapy plus conventional therapy
group Dconventional therapyTENS and cupping therapy plus conventional therapy
Primary Outcome Measures
NameTimeMethod
Visual Analog Scale (VAS)4 weeks
Pain-Free Grip Strength4 weeks
Patient-Rated Tennis Elbow Evaluation (PRTEE)4 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Bassam

🇪🇬

Qaliubia, Egypt

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