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Effect of Scapular Stabilization Exercise on Breastfeeding Women with Non-specific Neck Pain

Effect of Scapular Stabilization Exercise on Breastfeeding Women with Non-specific Neck Pain

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06817135
Enrollment
30
Registered
2025-02-10
Start date
2024-06-01
Completion date
2025-06-01
Last updated
2025-02-12

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

Conditions

Neck Pain

Keywords

scapular stabilization exercise, Breast feeding women

Brief summary

The purpose of this study is to determine whether scapular stabilization exercises can help breastfeeding women with non-specific neck pain by reducing their neck pain, cervical range of motion, and neck disability index.

Detailed description

The best infant feeding practice is breastfeeding, which has both immediate and long-term advantages for mothers, babies, the environment, the economy, and society as a whole. Mothers who are nursing frequently experience neck pain. Because the scapula and neck are closely related, scapular stabilization is becoming more and more popular for patients with neck pain.

Interventions

Cools exercise using the Thera-Band, including sidelying external rotation, side-lying forward flexion, prone horizontal abduction with external rotation, and prone extension exercises to promote lower trapezius and middle trapezius activity with minimal activation of the upper trapezius part.

OTHERMuscle Energy Technique

Muscle Energy Technique for the 1.sternocleidomastoid 2. levator scapulae 3. upper trapezius 4. pectoralis major Through mild isometric contractions, it uses the intrinsic energy of a muscle to lengthen it and induce relaxation through autogenic inhibition.

OTHERAdvice about the right the breastfeeding ergonomic.

The patients sit with their backs supported with pillows. Don't lean over the infant. Keep the arms supported and feet on the ground.

Sponsors

Saadyya Ahmed Abdalhamed Aladawi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

The control group got the standard physical therapy program, muscle energy technique for the sternocleidomastoid, elevator scapulae, upper trapezius, and pectoralis major, and advice, while the experimental group got the same conventional physical therapy program in addition to scapular stabilization exercises.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. exclusive breastfeeding mothers with immediate to 6-month-old infants. 2. The bilateral cradle position is employed by patients when nursing. 3. Patients had mechanical neck pain. 4. Patients with a body mass index below 30 kg/m² 5. Patients have moderate pain intensity, ranging from 3 to 7 on the visual analogue scale 6. The patients' scores on the Neck Disability Index ranged from 10 to 40 out of 50.

Exclusion criteria

1. Patients had preterm babies or low-birth-weight babies. 2. pregnant patients 3. Patients had postpartum complications. 4. Patients had inflammation, infection, severe degeneration, congenital deformity, and trauma. 5. Patients had sensory abnormalities or a positive motor reflex. 6. Patients had cancer, metabolic, or systemic diseases.

Design outcomes

Primary

MeasureTime frameDescription
functional neck disabilityat beginning of the study and after four weeks of treatmentThe Arabic version of the Neck Disability Index Questionnaire (NDI) is used to assess the functional neck disability. It consists of 10 items; each item scores from 0 to 5, where a score of 0 indicates no limitation and a score of 5 indicates maximum limitation.
neck pain intensityat beginning of the study and after four weeks of treatmentThe Visual Analog Scale VAS was used to assess neck pain intensity for both groups at the beginning of the study and after four weeks of treatment. It is a 10 cm line. 0 means no paint and 10 means maximum pain and the patient chooses a point on the line which reflects the pain

Secondary

MeasureTime frameDescription
cervical range of motionat beginning of the study and after four weeks of treatmentThe cervical range of motion (flexion, extension, lateral flexion (Rt & Lt), and rotation (Rt & Lt)) is measured with a universal goniometer.
pressure pain thresholdat beginning of the study and after four weeks of treatmentThe local pressure pain threshold over the upper trapezius was measured using a pressure algometer. It is a portable digital algometer that responds linearly to force applications between 0 and 1300 kPa, or roughly 0 and 14 kg. With a 1-cm² circular rubber tip, the device measures the maximum force applied before the subject verbally indicates that the pain threshold has been reached.

Countries

Egypt

Contacts

Primary ContactSaadyya A. Abdalhamed Aladawi, Asst Lect
dr.saadyya@gmail.com00201116364807
Backup ContactDr.Afaf M. Mahmoud Botla, Asst. Prof
drafafmohamed@yahoo.comAssistant Professor

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026