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Effect of Combined Application of Myofascial Release and Muscle Energy Technique on Pressure Pain Threshold in Patients with Myofascial Pain Syndrome after Breast Cancer Surgery

Effect of Combined Application of Myofascial Release and Muscle Energy Technique on Pressure Pain Threshold in Patients with Myofascial Pain Syndrome after Breast Cancer Surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011871
Enrollment
34
Registered
2026-04-17
Start date
2026-03-13
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

None listed

Interventions

Others(manual therapy technique (MyoFascial Release technique, Muscle Energy Technique)) : Participants’ general characteristics will be collected through electronic medical records (EMR). Baseline as

Sponsors

Gachon University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients who have undergone total mastectomy or partial mastectomy for breast cancer. 2. Patients presenting with a palpable taut band and a tender point upon examination. 3. Patients who report pain reproduction upon compression of the tender point. 4. Patients diagnosed with myofascial pain syndrome by a clinician. Participants were identified through electronic medical records (EMR) as patients diagnosed by a clinician. In cases where a formal diagnosis was not explicitly documented, individuals exhibiting clinical features consistent with myofascial pain syndrome were included based on assessment by a physical therapist with clinical experience.

Exclusion criteria

Exclusion criteria: 1. Patients with skin infection or inflammation. 2. Patients with contraindications to Myofascial Release (MFR) or Muscle Energy Technique (MET). 3. Patients who have difficulty maintaining the required position due to the presence of a chemoport or other medical devices. 4. Patients with lymphedema of stage II or higher. - Adverse Event Monitoring 1. Upper limb circumference will be measured using a tape measure before and after each intervention session. 2. Participants may be withdrawn from the study if edema persistently increases or worsens during the intervention period.

Design outcomes

Primary

MeasureTime frame
Pain Pressure Threshold

Secondary

MeasureTime frame
Shoulder Pain and Disability Index;European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30

Countries

Korea, Republic of

Contacts

Public ContactHONG DANBI

Gachon University

eksqldld@naver.com+82-32-820-4424

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Apr 23, 2026