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Evaluation of the effectiveness of symptom control in patients with cancer

Not Applicable
Conditions
Advanced Cancer.
Malignant neoplasm
C00-C97
Registration Number
IRCT20230408057851N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
90
Inclusion Criteria

Having a definite cancer diagnosis with the opinion of an oncologist
Physical and mental ability to communicate and complete questionnaires
Having a score of at least 4 in one of the annoying symptoms such as pain or other physical symptoms
Patient availability during the 2-week study period
First referral to the palliative care service

Exclusion Criteria

The patient is in the final phase of the disease
Prediction of survival of less than one month for the patient

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The intensity score of common symptoms experienced by cancer patients in the Edmonton Symptom Assessment Scale questionnaire. Timepoint: Time intervals for evaluation at the beginning of the study (before the cancer symptom management plan), and by passing 7, and 14 days from the intervention (Follow-up). Method of measurement: Edmonton Symptom Assessment Scale questionnaire (ESAS).;Quality of life in cancer patients. Timepoint: Time intervals for evaluation at the beginning of the study (before the cancer symptom management plan), and by passing 7, and 14 days from the intervention (Follow-up). Method of measurement: The European Organization for Research and Treatment of Cancer core quality of life questionnaire (EORTC-QLQ-C??).
Secondary Outcome Measures
NameTimeMethod
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