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Nursing intervention to reduce symptoms in cancer patients

Multimodal nursing intervention to reduce cancer treatment related symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9337nv
Enrollment
Unknown
Registered
2018-08-22
Start date
2016-05-23
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

Cancer

Interventions

Nursing Multimodal Intervention (experimental group): Education on symptom management, problem solving techniques and relaxation techniques. The experimental intervention (n=30) is applied in individu
Behavioural
Other
I02.233.332
G11.427.590.540.554
F02.463.425.725

Sponsors

Escola de Enfermagem da Universidade de São Paulo
Lead Sponsor
Instituto do Câncer do Estado de São Paulo
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactMarina;Marina Salvetti;Salvetti

Escola de Enfermagem da Universidade de São Paulo;Escola de Enfermagem da USP

mgsalvetti@usp.br;mgsalvetti@usp.br+55-011-30617558;3061-7558

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 24, 2026