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Manual Acupuncture Using Acupuncture Needle vs Press Needle for COVID-19 Healthcare Anxiety

Comparison of Manual Acupuncture Effectivity Using Filiform Needles and Press Tack Needle for Healthcare Worker's Anxiety During COVID-19 Outbreak: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04860271
Enrollment
36
Registered
2021-04-26
Start date
2021-03-09
Completion date
2021-05-31
Last updated
2022-03-08

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

Conditions

Anxiety

Keywords

acupuncture, press needle, anxiety

Brief summary

This study would like to compare manual acupunture treatment for anxiety in COVID Health workers population in Cipto Mangunkusumo Hospital using filiform needles and press needle.

Detailed description

This study wanted to know would press needle be having better outcome for anxiety treatment, compared with filiform needles, because press needle taken home and could be manipulated as needed at home, unlike filiform needle where an acupuncturist must be available to do the treatment. Furthermore, the press needle needed to be changed once within 5 days, that is 2-3 times in week. So we hope to have better acupuncture option (in effectivity and timewise) for COVID healthcare workers anxiety treatment. There are no study to compare the usage of the two types of needles for anxiety treatment to date.

Interventions

Manual acupuncture treatment using different types of needle

Sponsors

Indonesia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Investigator did not know the respondent and did not come in contact. The outcome assessor consist of 4 person who are randomly assessing the respondent, so the assessor do not know the full data since the beginning of participation thus do not have any bias when assessing the respondent

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* COVID-19 health workers. * Rapid test COVID-19 t or PCR swab non reactive within 7 days before intervention * HAM-A score below 25 * Could still do daily activities * Willing to enroll this study and sign the informed consent * Willing to comply with the study procedure

Exclusion criteria

* Contraindicated for acupuncture : having medical emergencies, pregnancy, blood clotting issue, uncontrolled diabetic mellitus, fever. * Having acupunture treatment within 7 days prior to study intervention * Having tumor or infection at the pucture site * Cognitive or consciouseness impairment * Having anxiety therapy with a psychiatrist

Design outcomes

Primary

MeasureTime frameDescription
Hamilton Anxiety Scaletwo weeksA questionnaire to access anxiety level, higher score means higher anxiety symptoms, ranged 0-56, mild anxiety scored below 17, 17-24 moderate anxiety, more than 24 severe anxiety
Short-Form 36two weeksA questionnaire to access quality of life, higher score means better quality of life. ranged 1-100. higher scores means better quality of life

Secondary

MeasureTime frameDescription
Heart Rate Variabilitytwo weeksA measurement to know the balance of autonomic nerve system

Countries

Indonesia

Outcome results

None listed

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