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ursing intervention to reduce symptoms in cancer patients

Not Applicable
Conditions
Cancer
pain
fatigue
sleep disturbance
anxiety
depression
C10.597.617
C23.888.369
F01.470.132
F01.145.126.350
Registration Number
RBR-9337nv
Lead Sponsor
Escola de Enfermagem da Universidade de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Data analysis completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Breast cancer; colorectal cancer or prostate cancer; be treated with chemotherapy or radiation; older than 18 years; minimum education of four years; not present language dysfunction and oriented in time and space.

Exclusion Criteria

Patients illiterate or with cognitive disabilities (dementia / psychosis); patients with high demand for care (Karnofsky score of <40).

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction of symptoms after the nursing intervention, verified through the application of the EORTC-QoL-C30 symptom scale, with a 20% reduction in the mean symptom score in the pre and post nursing intervention measurements.;There was a significant reduction in two post-intervention symptoms measured by the EORTC-QoL-C30 symptom scale: loss of appetite (59.7% reduction, p = 0.002) and insomnia (38.1% reduction in the score, p = 0.053). The other symptoms evaluated did not present a significant reduction after the intervention.
Secondary Outcome Measures
NameTimeMethod
Improvement of Quality of Life after the nursing intervention, verified through the application of the EORTC-QoL-C30 scale, with a 20% increase in the mean score of Quality of Life in pre and post measurements.;There was a 10% improvement in the quality of life score of the experimental group after the intervention, verified by the comparison of the EORTC-QOL-C30 score (p = 0.365) before and after the intervention. This difference was not considered significant.
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