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Investigation of the feasibility of acupuncture and moxibustion treatment on short-term intensive exercise program in care prevention

Investigation of the feasibility of acupuncture and moxibustion treatment on short-term intensive exercise program in care prevention - Investigation of the feasibility of acupuncture and moxibustion treatment on short-term intensive exercise program in care prevention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000049317
Enrollment
40
Registered
2022-10-25
Start date
2022-11-05
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

pain disorder

Interventions

Acupuncture treatment to the pain site complained by the subject. Acupuncture treatments will be performed once a week for a total of 14 treatments.

Sponsors

Aizu Medical Center, Fukushima Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Persons 65 years of age or older. 2 Those who have not received nursing care certification. 3 Gender is not a factor. 4 Subjects with chronic pain and VAS of 20mm or more.

Exclusion criteria

Exclusion criteria: 1 Research subjects with poorly controlled cancer. 2 Research subjects who have difficulty communicating due to mental disorders. 3 Research subjects with allergies to metals. 4 Research subjects who do not have pain. 5 Subjects with chronic pain but with a VAS of less than 20mm.

Design outcomes

Primary

MeasureTime frame
Evaluate the frequency of adverse events with respect to safety in the practice of acupuncture and moxibustion. Acupuncture treatments will be performed once a week for a total of 14 weeks, so the evaluation will be conducted in conjunction with each acupuncture treatment.

Secondary

MeasureTime frame
1. Assess the subject's pain using a visual analogue scale. 2. Quality of Life (QOL) assessment: QOL is assessed using the SF-8 (MOS 8-Item Short-Form Health Survey), with scores calculated from the SF-8. Secondary outcomes will be assessed at baseline (week 1) and at 16 weeks.

Countries

Japan

Contacts

Public ContactMasao Suzuki

Aizu Medical Center, Fukushima Medical University Department of Kampo Medical Research Institute

masuzuki@fmu.ac.jp0242752100

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026