Health Condition 1: null- before surgery and after surgery patient followup
Conditions
Interventions
Intervention1: NA: NA
Control Intervention1: NA: NA
Sponsors
Tata Memorial Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Pediatric solid tumor patients of either gender whose age is between 2-18 years who have been diagnosed and have consented to undergo treatment at Tata Memorial Centre after adequate staging workup
Exclusion criteria
Exclusion criteria: Patients who do not meet the above criteria. Patients unwilling to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Symptoms Scales i) Pain ii) Nausea iii) Anxiety iv) Worry 2 Functional scales i) Cognitive assessment ii) Perception of self body image iii) Communication Timepoint: There are no significant risks to the participants in this study. Patient might have tospend about 20-25 minutes for completing the Questionnaire | — |
Secondary
| Measure | Time frame |
|---|---|
| Though newer therapeutic options have resulted in improved health status of patients, the prolonged and frequent hospitalizations during this sensitive period of life could negatively impact child development. Also, in view of good survival, tools to assess clinical outcomes of different treatment modalities need to be developed. Therefore, there is focus on the developmentof instruments to assess health-related quality of life (HRQOL) outcomes.Timepoint: Assessing important side effects / complications following treatment for the medical professionals and step towards improving quality of life and minimizing the side effects. | — |
Countries
India
Contacts
Public ContactSwara Yogesh Jangam
Tata Memorial Hospital Parel Mumbai
Outcome results
None listed