Effect of Shockwave Therapy on Cervical Myofascial Syndrome in Lactating Women

NCT ID: NCT05878821

Last Updated: 2024-03-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-08-25

Study Completion Date

2023-09-25

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

the aim of the study is to determine the effect of shockwave therapy on cervical myofascial pain syndrome in lactating women

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Neck and shoulder pain was 73,1%,one fourth of which occurred after birth.the most common area was the superior part of the trapezius.the symptoms of patients are pain, stiffness and limited range of motion (ROM).

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cervical Myofascial Pain Syndrome

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two groups,one group will be treated by shockwave therapy and postural correction exercise and other group will be treated by postural correction exercise
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors
Double masking

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Postural correction exercise

All women in both groups (A\&B) will receive postural correction exercises which includes:

A.mckenzie exercises:

The exercise routine consists of seven types of movements,at static maximum strength, with 15\_20 repetitions, holding each repetition for seven seconds.the subjects complete one 20-minutes set per day,three times a week for four weeks B.strengthening exercise targeted the periscapular muscles (Y to W,l to W), scapular retraction.strengthening exercises will be progressively performed for 3sets, with 10 to15 repetitions C.pectoralis flexibility on a foam roller.Hold for 5seconds and repeated 10 time s

Group Type EXPERIMENTAL

Shockwave

Intervention Type DEVICE

Shockwave therapy session once a week for month 1000shock per session

Shockwave therapy

All women in group (B) will receive shockwave therapy once a week for the duration of the trial (4 weeks)

The dosage used will be as the following:

Energy flux Density (EFD)=0,25 ml/mm2 Number of shocks=1000 shocks(kamel et al.,2020). Time:2-5minutes per session.

Group Type EXPERIMENTAL

Shockwave

Intervention Type DEVICE

Shockwave therapy session once a week for month 1000shock per session

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Shockwave

Shockwave therapy session once a week for month 1000shock per session

Intervention Type DEVICE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Postural correction exercise

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Multipara two months after labor.
* number of parity not more than 3.
* age range 25\_35.BMI less than 35 Kg/m2

Exclusion Criteria

* Diabetic women
* Women with malignancy
* Neck pain from other conditions such as(spinal
* instability, spinal fracture, spinal cord compression,inflammatory disease, spinal infection, congenital postural deformity
Minimum Eligible Age

25 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Elham Shahat Hassan Baiuomy Ramadan

Lecturer of physical therapy Cairo university

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Faculty of physical therapy

Giza, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

P.T.REC/012/1004409

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.