Skip to content

A study comparing Gua Sha therapy and breast massage to reduce breast pain and fullness in mothers after childbirth.

Comparison of Gua Sha Technique and Therapeutic Breast Massage Technique for Treatment of Breast Engorgement in Postnatal Women A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096468
Enrollment
60
Registered
2025-10-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: O922- Other and unspecified disorders ofbreast associated with pregnancy and the puerperium

Interventions

Intervention1: Therapeutic Breast Massage Technique: The subject will be in a semi-reclined position with the breast properly exposed for intervention while maintaining the participant’s privacy. The

Sponsors

Dr Ritika Awate
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Postnatal lactating women 2) Able to give written informed consent 3) Having signs and symptoms of breast engorgement (pain, swelling, firmness of the breast tissue) 4) Scoring 2 and above on the point breast engorgement scale.

Exclusion criteria

Exclusion criteria: 1) Pre-existing breast conditions such as mastitis, abscesses, or a history of previous such conditions 2) Participants with a history of breast surgery (e.g., implants, reduction, or lumpectomy) 3) Women with severe postnatal complications (e.g., postpartum hemorrhage, preeclampsia) 4) Women on medications that affect lactation (e.g., lactation suppressants, hormone therapy) 5) Participants with open wounds, skin infections, or any dermatological conditions on the breasts 6) Non-cooperative patients 7) Medical conditions affecting circulation or requiring specific treatments 8) Women who are unable to give consent or participate due to language barriers or cognitive issues. 9) Participants who decline to provide informed consent or are unwilling to comply with the study requirements.

Design outcomes

Primary

MeasureTime frame
Six point breast engorgement scaleTimepoint: Pre intervention baseline, Post intervention immediately, 24 hours, post intervention fourth day

Secondary

MeasureTime frame
Numerical Pain Rating ScaleTimepoint: Pre intervention baseline, Post intervention immediately, 24 hours, post intervention fourth day

Countries

India

Contacts

Public ContactDr Ritika Awate

Terna Physiotherapy College

asawaripeter@ternapt.ac.in9960568048

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026