EHealth Educational Intervention to Improve Self-Management and Coping Behaviors Among Cancer Patients
EHCancer
A Controlled Evaluation of EHealth Interventions for Self-Management and Psychological Coping in Cancer Patients
1 other identifier
interventional
212
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable cancer
Started Nov 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 30, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 26, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 26, 2025
CompletedFirst Submitted
Initial submission to the registry
February 25, 2026
CompletedFirst Posted
Study publicly available on registry
March 9, 2026
CompletedMarch 9, 2026
February 1, 2024
3 months
February 25, 2026
March 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Symptom-Management Self-Efficacy Score
Measured using the Symptom-Management Self-Efficacy Scale (SMSE) developed by Liang et al. (2015). The scale consists of 27 items across three subscales: acquiring problem-solving (7 items), managing chemotherapy-related symptoms (15 items), and managing emotional and interpersonal disturbance (5 items). Each item is scored on an 11-point scale ranging from 0 (not at all confident) to 10 (completely confident). The total possible score ranges from 0 to 270. Higher scores indicate greater perceived self-efficacy in symptom management.
Baseline and 6 weeks (immediately post-intervention)
Secondary Outcomes (2)
Change in Coping Behavior Score
Baseline and 6 weeks (post-intervention)
Correlation Between Self-Efficacy and Coping Scores
6 weeks (post-intervention)
Study Arms (2)
Structured eHealth Intervention Group
EXPERIMENTALParticipants receive a structured eHealth educational intervention program delivered over six weeks in addition to routine care. The program focuses on enhancing self-management skills and psychological coping strategies among cancer patients.
Routine Care Control Group
NO INTERVENTIONParticipants receive routine care provided by the healthcare facility without additional eHealth educational intervention.
Interventions
The intervention consists of structured online educational sessions delivered via video conferencing platforms, supported by digital educational materials including videos and informational resources. The program incorporates scenario-based discussions, peer interaction, and continuous follow-up communication. The content focuses on symptom self-management, emotional regulation, and adaptive coping strategies for cancer patients.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Nursing
Zagazig, 44519, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This is an open-label study. Participants and investigators are aware of group assignments.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator, Professor, Nursing Administration, Faculty of Nursing, Zagazig University, Zagazig, Egypt.
Study Record Dates
First Submitted
February 25, 2026
First Posted
March 9, 2026
Study Start
November 30, 2023
Primary Completion
February 26, 2024
Study Completion
November 26, 2025
Last Updated
March 9, 2026
Record last verified: 2024-02