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Ort

Active, not recruiting • Phasen NA • Stufe 0, I, II, III, IV • ER negativ • Surgical • Post-Menopausal • Brain Metastases absent • Interventionell

Folgendes wird aus ClinicalTrials.gov importiert:

Acupressure for Cancer-Related Fatigue

This study develops and pilot tests the efficacy of a home-based, self-administered acupressure intervention in improving cancer-related fatigue (proximal outcome), and physical functioning and other quality of life outcomes (distal outcomes) of Chinese immigrant breast cancer survivors (versus usual care control group).

We will enroll 124 foreign-born, Chinese-speaking women from Southern California and Maryland areas with moderate to severe levels of fatigue, diagnosed with stage 0-IV breast cancer, aged 21-74, and 1-5 years post-primary treatment. Using an adaptive treatment strategy design, participants will be randomized to either the acupressure intervention or control groups. The acupressure group will learn how to press three chief energy acupoints on each side of the body through de novo 11-minute Chinese-language video and practice acupressure every day (one minute per acupoint; a total of 6 minutes per day) for an 8-week intervention period. Participants will be telephone interviewed twice: at baseline and 8-weeks post-intervention follow-up.

Breast Cancer

Studiendesign
Studientyp:

interventional

Geschätzte Einschreibung:

124 Teilnehmer

Aktueller Studienbeginn:

1. Juli 2016

Zulassungskriterien
Alter für die Studie berechtigt:

21 - 74

Geschlechter für die Studie berechtigt:

female


Arms and Intervention
  • acupressure intervention

  • usual care

Einschlusskriterien
  • 1) be between ages 21 to 74

  • 2) be first-generation immigrants

  • 3) speak Chinese (Mandarin and/or Cantonese)

  • 4) be diagnosed with breast cancer at stage 0, I, II III or IV

  • 5) have completed primary treatments (including surgery, radiation, and chemotherapy) 1-5 years prior to recruitment

  • 6) have not had recurrence

  • 7) have moderate to severe levels of fatigue.

Ausschlusskriterien
  • have hypothyroidism and anemia

  • being using acupuncture

Trial Information at Site
Last Updated:
Studieninformationen
ClinicalTrial.gov ID:

Active, not recruiting

Estimated Enrollment:

124

Last Updated:

12/07/2021


Hauptermittler

Judy Wang, Ph.D.


Studiensponsor

Georgetown University

Study Location (1)

Georgetown University

Washington, District of Columbia, United States

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