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Application of painting therapy in the treatment of acute chemotherapy induced nausea and vomiting (CINV) in patients with breast carcinomas

Application of painting therapy in the treatment of acute chemotherapy induced nausea and vomiting (CINV) in patients with breast carcinomas

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17010517
Enrollment
Unknown
Registered
2017-01-25
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Breast cancer

Interventions

experimental group:The patients were administered with painting therapy on the day of second chemotherapy cycle(painting booklet, whole body relaxation training,painting intentional guidance, and comp

Sponsors

CancerCenter, UnionHospital, Tongji Medical college, Huazhong University of Science and Tecchnology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
26 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. diagnosed withbreast carcinoma; 2. Aged>18 years old; 3. who planned to receive AC chemotherapy regimen for 4 cycles; 4. underwent chemotherapy forthe first time and had received AC chemotherapy regimen for one cycle; 5. used the unified antiemetic drugs; 6. degree of vomiting was GradeIIinthelast chemotherapy circle (The degree of vomiting had been classified as Grade0-IV according to the standard of World Health Organization. Grade0: no nausea and vomiting; GradeI: only nausea, no vomiting; GradeII: transient vomiting and nausea; GradeIII: vomiting in need of treatment; GradeIV: uncontrollable vomiting); 7. had the ability of reading and filling the questionnaires, and participated in this study voluntarily.

Exclusion criteria

Exclusion criteria: 1. who were poor, and the were not allowed to take part in this study; 2. who participated in other studies about psychological research at the same period; 3. who had mental retardation or mental illness; 4. whose clinical data was not complete.

Design outcomes

Primary

MeasureTime frame
FLIE scale;anxious;

Countries

China

Contacts

Public ContactPeng Xin

CancerCenter, UnionHospital, Tongji Medical college, Huazhong University of Science and Tecchnology

200507365@qq.com+86 15071399933

Outcome results

None listed

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