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A prospective randomized controlled clinical study on the impact of health promotion manual on the quality of life and mental health of HCC patients treated with radiofrequency ablation

A prospective randomized controlled clinical study on the impact of health promotion manual on the quality of life and mental health of HCC patients treated with radiofrequency ablation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012924
Enrollment
Unknown
Registered
2017-10-10
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-10-16

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

Conditions

Hepatocellular carcinoma

Interventions

trial group:distributing health promotion manuals for HCC patients who will be treated with radiofrequency ablation
control group:Not distributing health promotion manuals for HCC patients who will be treated with radiofrequency ablation

Sponsors

Xijing Hospital of The Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The maximum diameter of the tumor was 5 cm, or the tumor number was less than 3, the maximum diameter was less than 3 cm, and the postoperative pathology was hepatocellular carcinoma; 2. No vasculature and adjacent organ invasion; 3. Liver function grading Child A or grade B, or achieving the standard after internal medicine treatment; 4. Aged 18-80 years; 5. Being treated with ultrasound-guided radiofrequency ablation for the first time.

Exclusion criteria

Exclusion criteria: 1. Adjacent organ invasion or distant metastasis or merger of other tumors; 2. Tumor diameter >5 cm or with intrahepatic multiple metastasis; 3. A large amount of refractory ascites; 4. Mental disorders or psychological barriers; 5. Having a history of bleeding within one month before treatment; 6. Having the coagulant dysfunction that cannot be corrected; 7. Having a history of abusing alcohol or drugs or having poor compliance so that can not complete the follow-up according to the requirement.

Design outcomes

Primary

MeasureTime frame
Score of EORTC QLQ-30;

Secondary

MeasureTime frame
Score of SDS;Score of SAS;

Countries

China

Contacts

Public ContactYong Chen

Xijing Hospital of The Fourth Military Medical University

yongchen62@yahoo.com+86 13891915509

Outcome results

None listed

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