Education Impact on Family Health and Well-Being for Chemotherapy Patient Relatives
Structured Education Program for Caregivers of Chemotherapy Patients
Psychological Well-Being
+ Behavior
+ Personal Satisfaction
Supportive Care Study
Summary
Study start date: February 10, 2025
Actual date on which the first participant was enrolled.This study aims to explore how providing structured educational support to the family members of patients receiving chemotherapy can impact their overall health, eating habits, and mental well-being. The focus is on understanding if educating family members can help them manage stress better, improve their nutritional choices, and enhance their psychological state. Such education could be crucial in supporting families who are caring for loved ones undergoing cancer treatment, potentially leading to better overall family health and well-being. Participants in this study will be divided into two groups: one receiving the educational support and the other not. The education will include topics like self-confidence, healthy eating, and managing stress. The study will measure the effects using various tools at the beginning, middle, and end of the study period. These tools will assess changes in family health, adherence to a healthy diet, and levels of psychological well-being. The results will help determine if the educational program is beneficial in improving these aspects for the families involved. Statistical tests will be used to analyze the data and understand the outcomes of the educational intervention.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.171 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Van Yuzuncu Yil University Hospital
Van, Turkey (Türkiye)Open Van Yuzuncu Yil University Hospital in Google Maps