EHealth Educational Intervention to Improve Self-Management and Coping Behaviors Among Cancer Pat… (NCT07457112) | Clinical Trial Compass
CompletedNot Applicable
EHealth Educational Intervention to Improve Self-Management and Coping Behaviors Among Cancer Patients
Egypt212 participantsStarted 2023-11-30
Plain-language summary
Brief Summary This study evaluates the effectiveness of a structured eHealth-based educational and support intervention in improving self-management practices and psychological coping behaviors among adult cancer patients. Using a quasi-experimental pretest-posttest design with study and control groups, the intervention integrates online education, interactive sessions, and digital communication platforms to enhance symptom management, emotional regulation, and adaptive coping strategies. The findings aim to inform scalable digital health solutions in oncology care.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Male and female adult cancer patients
* Diagnosed with cancer and currently receiving chemotherapy
* Able to read and understand Arabic
* Own a mobile phone and able to use online applications (e.g., Zoom or similar platforms)
* Willing to participate in the eHealth educational program
* Provided informed consent to participate in the study
Exclusion Criteria:
* Patients with severe cognitive impairment or psychiatric disorders that interfere with participation
* Patients with critical health conditions preventing attendance in the intervention sessions
* Patients who participated in similar structured educational or coping programs during the study period
* Patients unwilling to complete baseline or follow-up assessments
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in Symptom-Management Self-Efficacy Score
Timeframe: Baseline and 6 weeks (immediately post-intervention)