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Digital Delivery of Patient Education: A Case Study of Symptom Self-Management During Cancer Treatment

Digital Intervention for Gastrointestinal (GI) Cancer Patients: A Case Study on Enhancing Symptom Self-Management During Treatment

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06187610
Enrollment
110
Registered
2024-01-02
Start date
2022-10-01
Completion date
2024-11-01
Last updated
2024-01-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Digital Education Interventions, Knowledge Types (Mechanistic Versus Procedural)

Brief summary

The increasing shift from face-to-face to online patient-clinician encounters in the healthcare system requires patients to be more involved in their medical care. This raises the urgent need to evaluate the extent to which proactive patients' self-care can be supported, particularly by informed telemedicine digital channels. Despite this imperative, research offering evidence-based instructional design of digital education remains surprisingly scarce. Embracing the framework of science education, which highlights the functional role of different knowledge types in educational processes, the current study seeks to evaluate an educational approach aimed at supporting cancer patients undergoing chemotherapy. Cancer treatment serves as an exemplar health condition, demanding daily self-management from patients. The objectives of our research are as follows: (1) To delineate the types of knowledge required for effective symptom management, active participation in one's healthcare, and judicious decision-making regarding emergency room (ER) visits, with a focus on mechanistic knowledge pertaining to the rationale for treatment and procedural knowledge concerning the treatment regimen. (2) To appraise the impact of a digital learning environment in contrast to traditional methods on patients' acquisition of mechanistic and procedural knowledge. (3) To identify how patients engage with the digital patient education environment aiming to outline leaning patterns. The investigators hypothesize that implementing digital education will enhance patients' understanding of both the 'why' (mechanistic) and 'how' (procedural) aspects of their treatment. Importantly, the investigators expect that mechanistic knowledge will be more impactful than procedural knowledge, leading to better symptom management and patient involvement, and ultimately reducing unnecessary visits to the ER.

Interventions

Patients assigned to the experimental group will learn about symptom self-management in a digital learning environment.

Sponsors

Weizmann Institute of Science
CollaboratorOTHER
Tel Aviv University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Gastrointestinal (GI) cancer patients * Chemotherapy session within a specific round of treatment, with eligible treatments including FOLFOX, FOLFIRINOX, and FLOT. * Hebrew speakers.

Exclusion criteria

* Impaired or degraded cognitive capabilities that may hinder effective learning. * Individuals who discontinue their treatments due to terminal advancement of their disease or death.

Design outcomes

Primary

MeasureTime frameDescription
Symptom self-management knowledgeThe test will be conducted in two time-points of the study, Time 0 (pre) and Time 2 (after two months)Measured by performance accuracy in a cancer-specific knowledge test

Secondary

MeasureTime frameDescription
Self-efficacy in symptom managementThe questionnaire will be administered three times: Time 0 (pre) and Time 2 (after two months)Measured by self-report Self-Efficacy for Managing Chronic Disease 6-Item Scale. The scale ranges from 1 (not confident) to 10 (very confident). A higher score is interpreted as a better self-efficacy.
Confidence in decision makingThe questionnaire will be administered in two time-points of the study, Time 0 (pre) and Time 2 (after two months)Measured by the self-report Decision Self-Efficacy Scale, which assesses patients' self-confidence in their ability to make decisions. It includes 11 items on a scale ranging from 0 (not at all confident) to 4 (very confident). A higher score is interpreted as higher confidence.
Patients engagement while learningon Time 2, namely about two weeks to four weeks after recruitmentPatients engagement with patient education material will be captured by psychophysiological parameters of eye-tracking and facial expressions

Countries

Israel

Contacts

Primary ContactIlana Dubovi
tairvi@gmail.com+97254-7922358

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026