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Acupressure for Pain and Opioid Use Among Breast Cancer Patients

NCT03655600 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2019-10-25

No results posted yet for this study

Summary

This study seeks to determine the feasibility of recruiting and training participants in self-acupressure, for women undergoing primary breast cancer surgery or delayed reconstruction surgery. The study seeks to determine also if self-acupressure is effective in reducing the need for opioids post-surgery and the effects on other life factors.

Conditions

Interventions

OTHER

Self-administered acupressure

Self-administered acupressure learned through app for reduction of need for opioids post-surgery in breast cancer patients

Sponsors & Collaborators

  • Substance Abuse and Mental Health Services Administration (SAMHSA)

    collaborator FED

  • Michigan Opioid Prescribing Engagement Network (Michigan-OPEN)

    collaborator UNKNOWN

  • University of Michigan

    lead OTHER

Principal Investigators

  • Suzanna M Zick, ND, MPH · University of Michigan

  • Richard E Harris, PhD · University of Michigan

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-17
Primary Completion
2019-10-17
Completion
2019-10-17

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03655600 on ClinicalTrials.gov