Fatigue As a Late Effect in Breast Cancer Survivors - is Acupuncture a Treatment Option?

NCT04418115 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 223

Last updated 2025-03-10

No results posted yet for this study

Summary

The success of treatment of breast cancer has improved, hence the prevalence of survivors have increased. However, experienced late effects from the cancer itself or from cancer treatment is substantial. Anti-cancer treatment can have a number of side effects including nausea, fatigue, vomiting, anorexia and alopecia. Late effects such as cancer related fatigue (CRF) are very persistent. CRF is a common side effect of cancer therapy, and affects the quality of life of patients and their families. It is important to point out that CRF is a form of fatigue that are different from normal fatigue which everyone can experience every now and then. Acupuncture is increasingly used in cancer centers both in the US and Europe, and that patients are positive to using acupuncture. Albeit the emerging evidence for acupuncture and CRF, acupuncture has neither been offered as a treatment for CRF within a Norwegian hospital nor in general practice. Hence the investigators think there is a need for a large randomized controlled trial (RCT) in a Norwegian health care setting.

Conditions

Interventions

OTHER

Acupuncture; based on Tradidtional Chinese Medicine

Acupuncture is a form of treatment that involves inserting very thin needles through a person's skin at specific points on the body, to various depths. Research suggests that it can help relieve pain, and it is used for a wide range of other complaints.

Sponsors & Collaborators

  • Norwegian Cancer Society

    collaborator OTHER
  • University of Bergen

    collaborator OTHER
  • Memorial Sloan Kettering Cancer Center

    collaborator OTHER
  • Dana-Farber Cancer Institute

    collaborator OTHER
  • University Hospital, Akershus

    collaborator OTHER
  • University of York

    collaborator OTHER
  • University of Tromso

    collaborator OTHER
  • Kristiania University College

    lead OTHER

Principal Investigators

  • Terje Alraek, PhD · School of Health Sciences, Kristiania University College

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2024-06-15
Completion
2024-12-31

Countries

  • Norway

Study Locations

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Entities

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 NCT04418115 on ClinicalTrials.gov