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Intervention of a Nursing Support Program for Work Continuation in Cancer Patients Undergoing Outpatient Treatment: A Randomized Controlled Trial

Intervention of a Nursing Support Program for Work Continuation in Cancer Patients Undergoing Outpatient Treatment: A Randomized Controlled Trial - Intervention of a Nursing Support Program for Work Continuation in Cancer Patients Undergoing Outpatient Treatment: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055961
Enrollment
30
Registered
2024-10-28
Start date
2024-11-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Cancer

Interventions

Individual consultations based on a nursing support program grounded in self-efficacy will be conducted by nurses. Control group: receives standard outpatient care and nursing as usual

Sponsors

Toho University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Cancer patients who are continuing to work 2)Aged between 18 and 65 years old 3)Patients who have started outpatient treatment within the last 6 months 4)Patients with an ECOG Performance Status of 0 or 1 5)Patients who have provided written consent to participate in this study 6)Patients who are capable of verbal communication in Japanese 7)Patients whose physical and mental condition allows for a 60 minute interview, as determined by the attending physician and nurse

Exclusion criteria

Exclusion criteria: 1)Individuals who will reach the mandatory retirement age during the study period 2)Individuals with cognitive impairments or other conditions that make verbal communication difficult 3)Patients scheduled for additional inpatient treatment, such as preoperative adjuvant therapy 4)Individuals whose condition has worsened due to cancer or other diseases, and whose prognosis is determined by the attending physician to be less than 6 months 5)Individuals deemed inappropriate by the principal investigator

Design outcomes

Primary

MeasureTime frame
Self-efficacy scale scores

Secondary

MeasureTime frame
1) Number and percentage of patients who completed each intervention 2) Employment status (working hours and days) 3) Quality of life (QOL) 4) Psychological stress

Countries

Japan

Contacts

Public ContactMasamitsu Kobayashi

Toho University Faculty of Nursing

masamitsu4k26@gmail.com03-3762-9236

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026