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NCT03173833 Clinical Trial

Fulfilling Care Needs of Adolescents With Cancer

Cancer Clinical Trial

Official title:
Fulfilling Care Needs of Adolescents With Cancer

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03173833
Other study ID # 201612238RINA
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 24, 2017
Last updated May 31, 2017
Start date August 1, 2017
Est. completion date July 31, 2020

Study information
Verified date April 2017
Source National Taiwan University Hospital
Contact Wei-Wen Wu
Phone 2312-3456
Email weiwen@ntu.edu.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of phase 1 of this study is to develop a care need scale (CNS) for adolescents with cancer. The aim of phase 2 is to examine the mediating role of care needs between physical and psychosocial dysfunction and QoL, and to explore the recovery trajectory and its predictors regarding the care needs, physical and psychosocial factors, and the QoL of adolescents with cancer at the first, second, and third 3-month periods after initiating on-treatment and off-treatment. The aim of phase 3 is to examine the effectiveness of the computerized assessment with graphic outcome (CAGO) for fulfilling the care needs of adolescents with cancer, its acceptability for adolescents with cancer, and its usability for clinicians in pediatric oncology units.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 720
Est. completion date July 31, 2020
Est. primary completion date July 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 13 Years to 20 Years
Eligibility The inclusion criteria for adolescents with cancer are

1. 13-20 years of age

2. previously or currently treated for cancer

3. able to communicate in Chinese

4. able to comprehend the study information

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• CAGO questionnaire outcome
Every time when cancer patients fulfill the following questionnaires, SDS, PTGI, CNS, PedsQL, the outcome of the questionnaires will be provided to the experimental group of the participants by using a computer assessment with graphic outcome.

Locations
Country Name City State
Taiwan National Taiwan University Hospital Test1 Test2

Sponsors (1)
Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Symptom Distress Scale 2 weeks
Primary Beck Youth Inventories second edition 2 weeks
Primary Posttraumatic Growth Index 2 weeks
Primary Resilience Scale 2 weeks
Primary Care demand scale 2 weeks
Primary Pediatric Quality of Life 2 weeks
Primary Acceptability if E-scale 2 weeks
Primary Usability scale 2 weeks
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