The Effect of Multimodal Approach of Electrotherapy Versus Shock Wave Therapy in Menopausal Women With Tennis Elbow.

ConditionShock Wave
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age45-55
SponsorOctober 6 University

About this trial

Tennis Elbow (or Lateral Epicondylalgia) is one of the most common overload injuries that it is the most frequent cause of lateral elbow pain, occurring to people between 40-60 years of age. It is characterized by pain on the outside of the elbow, usually near the lateral epicondyle bone where the extensor carpi Brevis tendon attaches, aggravated by gripping or wringing activities During menopause period, declining estrogen levels can negatively impact tendon health. Estrogen plays a protective role in tendons, contributing to their strength and ability to withstand load.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Patients with cervical radiculopathy ,thoracic outlet syndrome ,

dysfunction in shoulder or elbow with corticosteroid injection in previous three months.

Their BMI more than 25 kg/m2.

Unrelated to any traumatic conditions

Trial design

Design model

Single group

Treatments tested in this trial

  • multimodal electrotherapy

    Other intervention

    subjects will receive multimodal approach of electrotherapy (LLLT , and IFC) with conventional physical therapy modalities in the form of (stretch and strengthen exercises ) 3 sessions every week for 6 weeks

  • shock wave therapy

    Other intervention

    subjects will receive shock wave therapy with conventional physical therapy modalities 3 sessions every week for 6 weeks.

  • exercise

    Other intervention

    subjects will receive with conventional physical therapy modalities only in the form of (stretching and strengthening therapeutic exercises ) 3 sessions every week for 6 weeks.

Treatment groups

45 Participants
are divided into 3 treatment groups
Group A: Group AExperimental treatment 1 intervention
Group B: Group BExperimental treatment 1 intervention
Group C: Group CExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Visual analogue scale

The VAS consists of a 10-cm line, with the left extremity indicating ''no pain'' and the right extremity indicating ''unbearable pain.'' Participants asked to use the scale to indicate their current level of pain Higher values suggest more intense pain ,It was found that VAS provide valid and reliable assessments for the affective magnitude, as well as the sensation intensity of pain.

Time frame
6 weeks
2

hand grip

Grip hand strength will be assessed by hand held dynamometer

Time frame
6 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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