Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 4:18 AM
Ignite Modification Date: 2025-12-25 @ 4:18 AM
NCT ID: NCT04822220
Eligibility Criteria: Inclusion Criteria: * Inpatients for symptom management or supportive care in oncology wards * Patients who were at first two days of hospitalization * Patients who had score of 3≤ or ≤7 in Fatigue Visual Analogue Scale (VAS) * Patients who had score of ≤5 in Pain Analog Visual Scale (VAS) * Patients who had score of ≤5 The Modified Borg Scale * Patients who had score of 0, 1, 2 or 3 in ECOG Performance scale * Patients who had metastases * Patients who were over 18 years of age * Patients who had orientation of person, place and time * Patients who had no communication barriers * Patients who agreed to participate in the study Exclusion Criteria: * Patients who had hospitalized for the purpose of receiving chemotherapy * Patients whose Hb value was ≤8 g / dl * Patients whose body temperature ≥ 38.5 ° C within the last 24 hours * Patients who had diarrhea in the last 24 hours (frequency of defecation ≥ 3 / day) * Patients who had a score of ≤ 16 kg / m2 in Body Mass Index (BMI) * Patients who had advanced heart failure * Patients who had untreated hypothyroidism * Patients who diagnosed with major depression and / or treated for depression * Patients who had no family member involved in their care
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT04822220
Study Brief:
Protocol Section: NCT04822220