Muscle Energy Technique Versus Mulligan Technique for Treating Neck Pain in Breast Feeding Women

Neck Pain Clinical Trial

Official title:

Muscle Energy Technique Versus Mulligan Technique for Treating Neck Pain in Breast Feeding Women

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04930575
• Other study ID #: HElbasiony_MSc
• Status: Recruiting
• Phase: N/A
• Start date: March 1, 2021
• Est. completion date: June 30, 2021

Study information

• Verified date: June 2021
• Source: Cairo University
• Contact: Heba Elbasiony, Physical Therapist
• Phone: +201007065666
• Email: mheba7033[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study will determine the effect of muscle energy technique versus mulligan technique on neck pain in breastfeeding women.

Description:

Conservative treatments used to manage neck pain are numerous and include usual medical care ( face to face interview, education, reassurance, medication, ergonomic and stay active advice), various forms of exercise, massage, and acupuncture among others, but a lack of evidence regarding their relative efficacy was found. More research is needed to determine specific exercise programs that can decrease neck pain in breastfeeding women. So, this study will be conducted to determine clinical evidence of the effectiveness of muscle energy technique versus mulligan technique on neck pain, which constituted a great problem facing the mother during the breastfeeding period.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 32
• Est. completion date: June 30, 2021
• Est. primary completion date: June 15, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 25 Years to 35 Years

Eligibility

Inclusion Criteria:

• Patients will be examined by a physician before the study and will be chosen according

to the following criteria:

• All patients will be in the breastfeeding period at least 6 weeks after delivery.
• All patients will be clinically diagnosed with neck pain (with no neurological or rheumatological problem).
• Their ages will range from 25-35years.
• Their BMI will be less than 30 kg/m².
• Their parity will not be more than 3 times.

Exclusion Criteria:

• The patients will be excluded if they have any of the followings:

1. Any contraindication to spinal mobilization (e.g., inflammation, infection, advanced degeneration, congenital malformation, trauma, cerebrovascular abnormalities).

2. Positive neurological examination (presence of positive motor reflex, or sensory abnormalities indicating spinal root compression).

3. Cervical spine surgery or stenosis, metabolic or systemic disorder, or cancer.

4. Associated pathology of the upper cervical region or upper limb that may cause overlapping with the clinical finding as referred pain from the costotransverse joint, rotator cuff tendonitis, and cervical rib syndrome.

Related Conditions & MeSH terms

• Breast Feeding
• Mastodynia
• Neck Pain

Intervention

Other:
• Muscle Energy Technique
A biomechanical correction approach can lead to the normalization of spinal curvatures and a decrease in the compressional and tensional stress on joints and soft tissues of the body.
• Mulligan Technique
The patient will be in a supportive low back chair, thus cervical region will be in a vertical position (Weight-bearing position) with the therapist position will be behind the patient. Then the therapist will move the spinous process up in the direction that must follow the apophyseal joint plane under treatment, that is, toward the eye ball. While sustaining this pain-free accessory glide, the patient will be instructed to actively perform the physiological movement gradually until the end ROM with over pressure at the end of the range.

Locations

Country	Name	City	State
Egypt	Faculty of Physical Therapy Cairo University	Dokki

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessing the change in Cervical pain level	Assessment via using Visual Analogue Scale that continuous data analysis and uses a 10 cm long with 0 (no pain) and 10 (worst pain). Patient will be asked to place a mark along the line to denote their level of pain.	Baseline and 4 weeks post-intervention
Primary	Assessing the change in Functional disability	Assessment via using Neck pain disability index questionnaire consists of 10 items each of them is scored from 0 to 5. The total maximum score is therefore 50.The original report provided scoring interval for interpretation, as; (0-4) = no disability, (5-14) mild, (15-24) moderate, (25-34) sever, (above34) complete disability.	Baseline and 4 weeks post-intervention
Primary	Assessing the change in Cervical Range Of Motion	Assessment via using Digital goniometer is valid and has good reliability for measuring cervical spine range of motion.	Baseline and 4 weeks post-intervention