Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06188286

The Effect of Patient-Controlled TEAS vs Sham TEAS for Improve Quality of Life in Patients With Cancer Pain

Patient-Controlled Transcutaneous Acupoint Electrical Stimulation to Improve Quality of Life in Patients With Cancer Pain

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
94 (estimated)
Sponsor
Yi Liang · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The conduct of a pilot trial is of great significance as a means of assessing the feasibility and harmonization of the research and is a very necessary precursor to the better conduct of formal trials. The primary aim of this pilot study is to assess the feasibility of a PC-TEAS in improving the quality of life of cancer patients with pain, with the aspiration of providing process evidence base and an assessment of the intervention for conducting a formal trial. the secondary outcome is to assess the clinical efficacy of the PC-TEAS.

Conditions

Interventions

TypeNameDescription
OTHERTranscutaneous electrical acupoint stimulationThe 4 patches of the transcutaneous acupoint electrical stimulator were pasted on two pairs of acupuncture points, the output frequency was adjusted to 2Hz, the intensity was up to 50ma, the single intervention time was 30 minutes, and another group of acupuncture points was replaced after completion, and the rest of the operations were the same as above, with a total intervention time of 1 hour.
OTHERsham Transcutaneous electrical acupoint stimulationThe patch is fixed on the acupuncture point to turn on the instrument, but there is no current output

Timeline

Start date
2024-12-25
Primary completion
2025-10-31
Completion
2025-12-30
First posted
2024-01-03
Last updated
2024-12-24

Source: ClinicalTrials.gov record NCT06188286. Inclusion in this directory is not an endorsement.