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A prospective cohort study on the effectiveness of different acupoint stimulation therapies in alleviating symptoms of diabetic distal symmetric polyneuropathy

A prospective cohort study on the effectiveness of different acupoint stimulation therapies in alleviating symptoms of diabetic distal symmetric polyneuropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025000508
Enrollment
Unknown
Registered
2025-03-11
Start date
2025-03-31
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Diabetic distal symmetric polyneuropathy

Interventions

Home-based transcutaneous electrical stimulation group:Home-based transcutaneous electrical stimulation
Electroacupuncture combined with auricular acupoint pressing group:Electroacupuncture combined with auricular acupoint pressing once a week
Electroacupuncture group:Electroacupuncture three times per week

Sponsors

School of Acupuncture-Moxibustion and Tuina Beijing University of CM Beijing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for DSPN. 2. Aged between 18 and 75 years. 3. Voluntarily participate in the study and sign an informed consent.

Exclusion criteria

Exclusion criteria: 1. Unhealed foot ulcers gangrene or amputation of limbs/toes. 2. Implantation of a cardiac pacemaker. 3. Pregnancy breastfeeding or planned pregnancy. 4. Diagnosis of malignant tumors undergoing chemotherapy severe cardiovascular or cerebrovascular diseases infectious diseases liver and kidney dysfunction alcohol abuse etc. 5. Diagnosis of malignant tumors undergoing chemotherapy severe cardiovascular or cerebrovascular diseases infectious diseases liver and kidney dysfunction alcohol abuse etc. 6. Cognitive dysfunction aphasia mental disorders or other conditions preventing cooperation with the study.

Design outcomes

Primary

MeasureTime frame
Total Symptom Score (TSS);

Secondary

MeasureTime frame
Patient Health Questionnaire (PHQ-9) score;Beck Anxiety Inventory(BAI) score;Score of sensory symptoms on the TSS scale;Numerical Rating Scale(NRS) score;Skin burning symptom score of TSS scale;Pain symptom score on the TSS scale;Numbness symptom score of TSS scale;Nerve Conduction Study;Pittsburgh Sleep Quality Index(PSQI) score;EuroQol Five-dimensional Five-level Questionnaire(EQ-5D-5L) score;

Countries

China

Contacts

Public ContactShiyan Yan

School of Acupuncture-Moxibustion and Tuina Beijing University of CM Beijing

zc13309604509@163.com13681213627

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026