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

ConditionCancer Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorYi Liang

About this trial

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.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Transcutaneous electrical acupoint stimulation
  • sham Transcutaneous electrical acupoint stimulation

Treatment groups

94 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Yi Liang

Lead sponsor

The Third Affiliated hospital of Zhejiang Chinese Medical University

Sponsor institution