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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

The inclusion of non-drug therapy in the nursing process for the management of emesis and mucositis in patients with breast and lung Cancer submitted to chemotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3q2c68
Enrollment
Unknown
Registered
2018-02-06
Start date
2017-10-20
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emesis and mucositis caused by chemotherapy in patients with breast or lung cancer.

Interventions

The study will be carried out in the oncology department of Botucatu State Hospital and home visits to patients in the cities belonging to the Polo Cuesta, which comprises 13 cities: Anhembi, Areiópol
Device
Other
G07.203.100.975
E02.258

Sponsors

Departamento de Enfermagem da Universidade Estadual de São Paulo
Lead Sponsor
Universidade Estadual de São Paulo
Collaborator
Departamento de Enfermagem da Universidade Estadual de São Paulo
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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. 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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactAngela;Angela Martini;Martini

Universidade Estadual de São Paulo;Universidade Estadual de São Paulo

amartini@fmb.unesp.br;amartini@fmb.unesp.br+55143880-1328;+55143880-1328

Outcome results

None listed

Source: REBEC (via WHO ICTRP)