Actively Recruiting

Phase 3
Age: 18Years +
All Genders
Healthy Volunteers
NCT06859190

Efficacy of Auricular Pressure Beans with Electroacupuncture and Estazolam Treating Insomnia Caused by Cancer

Led by Qinghai Red Cross Hospital · Updated on 2025-03-25

60

Participants Needed

1

Research Sites

91 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The core objectives of this study are to assess the short-term and long-term efficacy of auricular acupoint pressure beans combined with electroacupuncture and estazolam in the treatment of cancer-caused insomnia. The study aims to accurately compare the differences between this combination therapy and standard Western medicine in improving sleep quality and effectively alleviating anxiety and depression. Additionally, it will meticulously observe the safety of the combined treatment and record the occurrence and potential causative factors of any adverse reactions.

CONDITIONS

Official Title

Efficacy of Auricular Pressure Beans with Electroacupuncture and Estazolam Treating Insomnia Caused by Cancer

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 and above.
  • Confirmed diagnosis of malignant solid tumor by pathological examination.
  • Cancer-caused insomnia symptoms lasting more than 1 month, occurring 3 or more times per week.
  • Insomnia Severity Index (ISI) score of 8 or higher and meeting insomnia disorder criteria in DSM-5.
  • No use of insomnia-related medications in the last 1 month.
  • No serious dysfunction of heart, liver, kidneys, or other vital organs.
  • Volunteered for the study and signed informed consent form.
Not Eligible

You will not qualify if you...

  • Irregular sleep-wake cycles due to shift work or inconsistent schedules.
  • Untreated or inadequately treated other sleep disorders such as sleep apnea or restless leg syndrome.
  • Received acupuncture or auricular pressure bean therapy within the past 3 months.
  • Estimated life expectancy of 3 months or less.
  • History of severe allergies to drugs or treatments used in this study.
  • History of severe mental illness with a current episode.
  • History of substance abuse or alcohol dependence.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

China, Qinghai,Qinghai Red Cross Hospital

Xining, Qinghai, China, 810000

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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