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Health education of patients with gastrointestinal neoplasia in antineoplastic chemotherapy and quality of life, functional capacity and fatigue

Health education on quality of life, functional capacity and fatigue of patients with digestive system neoplasia in antineoplastic chemotherapy: a quasi experimental study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4zkjfx
Enrollment
Unknown
Registered
2019-12-03
Start date
2019-04-01
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

Pharmacological treatment

Interventions

The intervention was designed based on psychoeducation and the Cognitive Behavioral Therapy (CBT) was used as a theoretical model to support the intervention including training in problem solving, the
Other
I02.233.332

Sponsors

Universidade Federal do Triângulo Mineiro
Lead Sponsor
Universidade Federal do Triângulo Mineiro
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: The study will include patients diagnosed with CA of the digestive system aged 18 years or older undergoing intravenous antineoplastic chemotherapy treated at the HC / UFTM chemotherapy service. To this end, they agreed to participate in the study by signing the Informed Consent Form, as well as the Free Informed Consent Form prepared according to Resolution 466/12 of the National Health Council (BRAZIL, 2012).

Exclusion criteria

Exclusion criteria: Will be excluded from the study patients who underwent antineoplastic chemotherapy treatment and / or previous radiotherapy; in adjuvant radiotherapy treatment; diagnosis of metastatic AC, which will perform less than three treatment cycles and / or change chemotherapy protocol during the study.

Design outcomes

Primary

MeasureTime frame
It is expected to find a reduction and / or a better fatigue score in the intervention group compared to the control group, verified by the Piper Fatigue Scale, the results are presented by percentages used to verify if the outcome actually occurred

Secondary

MeasureTime frame
It is expected to find an increase and / or better quality of life score in the intervention group compared to the control group, to be evaluated by the EORTC-QLQ-C30, the results will be presented by percentages used to verify if the outcome actually occurred

Countries

Brazil

Contacts

Public ContactElizabeth Barichello

Universidade Federal do Triângulo Mineiro

lizabarichello@hotmail.com55 34 991740297

Outcome results

None listed

Source: REBEC (via WHO ICTRP)