NCT07457112

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
212

participants targeted

Target at P75+ for not_applicable cancer

Timeline
Completed

Started Nov 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 30, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 26, 2024

Completed
1.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 26, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

February 25, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

March 9, 2026

Completed
Last Updated

March 9, 2026

Status Verified

February 1, 2024

Enrollment Period

3 months

First QC Date

February 25, 2026

Last Update Submit

March 3, 2026

Conditions

Keywords

EHealthSelf-ManagementEducational Intervention

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

EXPERIMENTAL

Participants 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.

Behavioral: Structured eHealth Educational Intervention

Routine Care Control Group

NO INTERVENTION

Participants 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.

Structured eHealth Intervention Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

NeoplasmsColonic NeoplasmsBreast NeoplasmsLymphomaMultiple Myeloma

Condition Hierarchy (Ancestors)

Colorectal NeoplasmsIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesNeoplasms by Histologic TypeLymphoproliferative DisordersLymphatic DiseasesHemic and Lymphatic DiseasesImmunoproliferative DisordersImmune System DiseasesNeoplasms, Plasma CellHemostatic DisordersVascular DiseasesCardiovascular DiseasesParaproteinemiasBlood Protein DisordersHematologic DiseasesHemorrhagic Disorders

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
Model Details: Participants receive a structured eHealth intervention over 6 weeks, including: * Online educational sessions (Zoom / Google Meet) * Digital learning materials (videos, posters, pamphlets) * Scenario-based discussions and peer interaction * Continuous communication and reminders via WhatsApp * Focus areas: symptom self-management, emotional regulation, adaptive coping strategies Control Group Participants receive standard educational materials only (limited sessions without interactive eHealth components).
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

Locations