Status:

COMPLETED

The Impact of Oral Cryotherapy and Chewing Gum Interventions

Lead Sponsor:

Hacettepe University

Conditions:

Breast Cancer

Nausea and Vomiting

Eligibility:

FEMALE

18-65 years

Phase:

NA

Brief Summary

Chemotherapy-induced nausea and vomiting (CINV) and taste alterations continue to be among the most common and most severe side effects that women receiving adjuvant chemotherapy for breast cancer suf...

Detailed Description

Chemotherapy-induced nausea and vomiting (CINV) remains one of the most distressing and prevalent side effects of cancer treatment, affecting a substantial proportion of patients undergoing chemothera...

Eligibility Criteria

Inclusion

  • Women aged between 18 and 65 years,
  • Scheduled to receive adjuvant chemotherapy for the first time,
  • Receiving the AC protocol as their chemotherapy regimen,
  • Receiving chemotherapy doses classified as moderately emetogenic (according to the International Society of Supportive Care in Cancer Guidelines),
  • Not having received radiotherapy prior to adjuvant chemotherapy,
  • Without chronic diseases (coronary artery disease, chronic kidney disease, or diabetes mellitus),
  • Not having used any non-pharmacological method for nausea and vomiting,
  • Diagnosed with breast cancer for the first time,
  • Without metastasis,
  • Without thrombocytopenia,
  • At an early stage,
  • Aware of their diagnosis,
  • Open to communication and cooperation,
  • Literate,
  • Not receiving psychiatric and/or depression treatment,
  • Not in the terminal stage,
  • Willing and volunteering to participate in the study.

Exclusion

  • Illiterate,
  • Over 65 years of age,
  • Using anxiolytic or antidepressant medications,
  • Having chronic diseases (gastrointestinal obstruction/disease, hepatitis, coronary artery disease, chronic kidney disease, or diabetes mellitus),
  • Having metastasis,
  • Having received radiotherapy prior to adjuvant chemotherapy,
  • Not willing to participate in the study.

Key Trial Info

Start Date :

June 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2022

Estimated Enrollment :

135 Patients enrolled

Trial Details

Trial ID

NCT07145320

Start Date

June 1 2021

End Date

May 1 2022

Last Update

August 28 2025

Active Locations (1)

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Hacettepe University

Ankara, Adnan Saygun, Turkey (Türkiye), 06100