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Electro-acupuncture for cancer-related cognitive impairment

Electro-acupuncture for cancer-related cognitive impairment: a single group, before-after, feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002168
Enrollment
15
Registered
2016-12-09
Start date
2016-11-28
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Procedure/Surgery : Electro-acupuncture will be performed twice a week for 8 weeks, total 16 times.

Sponsors

Korea Institute of Oriental Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged equal to or more than 19 to under 75 years 2. solid cancer occured in adult age, 6 months after finishing cancer treatment (hormone therapy is allowed) 3. Complaint of cognitive impairment with The functional assessment of cancer therapy-cognitive function-perceived cognitive impairments (FACT-cog-PCI score) <63 4. Cognitive impairment is suppose to be accompanied with cancer treatment 5. Eastern cooperative oncology group (ECOG) performance status 0~2 6. agreed with written informed consent

Exclusion criteria

Exclusion criteria: 1. currently receiving any of cognitive rehabilitation therapy, herbal medicine or conventional treatment for cognitive impairment; or having experiences of those treatment within 2 weeks 2. history of tumor in central nervous system (CNS), intra-cranial radiotherapy, or intrathecal chemotherapy; or history of CNS diseases which can affect cognitive function 3. Recurrence, metastasis or progression of cancer 4. history of psycological disorders including alcohol dependence, major depressive disorder, schizophrenia or bipolar disorder 5. Korean Vision of Mini-Mental State Exam (K-MMSE) score 10,000/µL 10. serum albumin value under normal range and poor oral intake 11. seriously unstable medical condition such as abnormal condition demanding medical intervention or management 12. life expectancy = 6 months 13. planning operation, chemotherapy or radiotherapy during the clinical trial period 14. receiving active treatment for anemia (erythropoietin or blood transfusion) 15. history of hypersensitivity reaction to acupuncture or electroacupuncture; or difficult to cooperate for the intervention 16. inserted prosthesis which is inappropriate for electroacupuncture (pace maker, a heart-lung machine, an electroacrdiograph etc.), or who has possibility of hypersensitivity reaction to electroacupuncture including epilepsy 17. currently being enrolled on another clinical trial or it is not passed 4 weeks after completion of previous clinical trial 18. pregnant women, lactating women, or planning for pregnancy 19. difficult to comply the treatment, visit or reponse to questionnaires etc.

Design outcomes

Primary

MeasureTime frame
Functional Assessment of Cancer Therapy-Cognitive Function (Fact-Cog)

Secondary

MeasureTime frame
European Organization for Research and Treatment of Cancer Quality of Life Core Questionnaire C30 (EORTC-QLQ-C30);Korean version of Montreal Cognitive Assessment (MoCA-K);Hospital anxiety and depression scale (HADS);The Seoul Neuropsychological Screening Battery (SNSB);Measure Yourself Medical Outcome Profile (MYMOP V2);Adverse event

Countries

Korea, Republic of

Contacts

Public ContactJeong-hyo Cho

Daejeon Korean Medicine Hospital of Daejeon University

choajoa@dju.kr+82-42-229-6806

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 13, 2026