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Cancer symptom management system: the system development and feasibility evaluation

Cancer symptom management system: the system development and feasibility evaluation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002096
Enrollment
324
Registered
2016-10-07
Start date
2015-12-17
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

None listed

Interventions

Others : Control group only receives symptom monitoring utilizing study-developed symptom management system. Experimental 1 group receives symptom monitoring and symptom report will be delivered to

Sponsors

Chungnam National University
Lead Sponsor
Yonsei University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult (19 years or orlder) cancer patients who were diagnosed with stomach, breast, colorectal, or lung cancer Planned to start adjucant or palliative chemotherapy of at least 4 cycles (for pilot trial of the system, Adult cancer patients who were diagnosed with stomach, breast, colorectal, or lung cancer and receiving adjuvant or palliative cancer or any cycle). Licensed clinicians (MD or RN), currently working medical oncology or caring for oncology patients with at least 2 years of clinical experience in the field, and providing chemotherapy and manage symptoms.

Exclusion criteria

Exclusion criteria: Patients who receive chemotherapy accompanied with surgery or radiation therapy Patients who have cognitive or psychiatric problems which might hinder study participation

Design outcomes

Primary

MeasureTime frame
Effect in symptom management: changes in symptom severity

Secondary

MeasureTime frame
Validity and Reliability of symptom management system;Quality of life;Feasibility;Patient satisfaction

Countries

Korea, Republic of

Contacts

Public ContactJiyeon Lee

Chungnam National University

jiyeonest@hotmail.com+82-42-580-8320

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026