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The inclusion of non-drug therapy in the Nursing Process for the control of nausea / vomiting and mouth sores in patients with breast and lung Cancer undergoing chemotherapy

Not Applicable
Recruiting
Conditions
Emesis and mucositis caused by chemotherapy in patients with breast or lung cancer.
C04.588.894.797.520
C34.3
C34.2
C34.1
C04.588.180
E02.183.750
Registration Number
RBR-3q2c68
Lead Sponsor
Departamento de Enfermagem da Universidade Estadual de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Over 18 years of age;both genders;carrier of breast or lung cancer;being in adjuvant or neoadjuvant chemotherapeutic treatment;being the first chemotherapy treatment performed;to be performing the first 4 cycles of chemotherapy in the State Hospital of Botucatu.

Exclusion Criteria

Patients in palliative care;patients refuse to participate in the research;who not in the first 4 cycles of chemotherapy;patient with recurrence of breast and lung cancer;withdrawal of treatment;death.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The management of emesis and mucositis in patients with breast or lung cancer who underwent chemotherapeutic treatment through the use of ginger tea and mouthwash with chamomile tea, respectively.<br>It will be evaluated through the collection of data that is performed by telephone to analyze adherence and decrease the incidence of adverse reactions. It was done 72 hours after the consumption of ginger tea and for evaluation of the effect of the mouthwash with chamomile tea and researcher will contact on the 10th day. At the end of the interventions and data collection, a statistical analysis of the data is performed.
Secondary Outcome Measures
NameTimeMethod
Individualized treatment variables may interfere with the study: the impact of interventions according to each type of neoplasm (breast or lung) and the prescribed chemotherapy, personal characteristics of each patient (oral hygiene, oral characteristics or changes prior to chemotherapy treatment , eating habits, pathologies concomitant with carcinoma, parallel therapies). These aspects will be evaluated through oral cavity evaluation and anamnesis, for further comparison of the data and identification of interferences in the study.
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