Press Needle Acupuncture for Pain and Quality of Life in Lung Cancer Patients

University of Indonesia (UI)

Status: Not yet enrolling

Conditions: Lung Cancer Patients

Treatments: Device: Press Needle Acupuncture and standart therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT07112950

25-05-0758

Details and patient eligibility

About

The purpose of this clinical trial is to evaluate the effect of press needle acupuncture on pain management and quality of life improvement in patients with lung cancer.

The main question this study aims to answer is:

Does press needle acupuncture, when combined with standard therapy, provide better pain relief and quality of life improvement in lung cancer patients compared to standard therapy alone?

Researchers will compare press needle acupuncture to sham acupuncture to determine whether press needle acupuncture is more effective in reducing pain and improving quality of life.

Participants will:

Receive either press needle acupuncture or sham press needle acupuncture for 7 days

Visit the clinic once a week for examination and evaluation

Record improvements in pain intensity in a pain diary and assess quality of life using a quality of life questionnaire

Enrollment: 32 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with a confirmed diagnosis of lung cancer through histopathology or radiology.
• Lung cancer patients aged over 18 years.
• Stage III-IV lung cancer patients receiving therapy at Dr. Cipto Mangunkusumo National General Hospital (RSUPN) and Tangerang District General Hospital (RSUD Kabupaten Tangerang).
• Patients with a VAS score >10 mm for baseline pain and >40 mm during breakthrough pain.
• Willing to participate in the study until completion by signing the informed consent form.

Exclusion criteria

• Lung cancer patients with deteriorating general condition.
• Presence of wounds or infections at the press needle insertion site.
• History of allergy to stainless steel materials.
• Patients with blood clotting disorders: platelet count <50,000/μL, ANC <1000/mm³, or patients undergoing anticoagulant therapy with INR >2.142.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Triple Blind

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32 participants in 2 patient groups

Intervention Group

Experimental group

Description:

The press needle acupuncture and standart therapy

Treatment:

Device: Press Needle Acupuncture and standart therapy

Control Group

Sham Comparator group

Description:

The sham press needle acupuncture and standart therapy

Treatment:

Device: Press Needle Acupuncture and standart therapy