Does the Level of Pain in Pediatric Oncology Patients Affect the Level of Psychological Resilience in Parents?

NCT06445816 | Active Not Recruiting DMC

• 1 other identifier: Istanbul Gelişim Üniversity
• Study Type: observational
• Target: 50
• Locations: 1 country
• Sites: 1

Brief Summary

Resilience is defined as generating coping strategies for the problems and situations that individuals face throughout their lives and developing these strategies in each new situation. While some individuals become helpless in the face of difficulties and give up the struggle, other individuals recover quickly in the face of difficulties and use coping methods well. Accordingly, these individuals have higher levels of crisis management and coping with stress.

Conditions

Pain; Pediatric Oncology; Psychological Resilience

Outcome Measures

Primary Outcomes (1)

• Psychological resilience scale

  The pain level of the child receiving chemotherapy will reduce the psychological resilience of the mother. In the schematic evaluation, the scoring method is free for measuring psychological resilience as high or low.

  2 day

Interventions

chemotherapy DRUG

* Parents whose consent was obtained will be asked to fill out the Mother and Child Information Collection Form and Psychological Resilience Scale, respectively. * Immediately after receiving chemotherapy, the pain levels of the children will be measured with the Facial Expressions Pain Scale - Faces Pain Scale-Revised (FPS-R). * The psychological resilience scale will be applied to mothers.

Eligibility Criteria

• Age: 4 Years - 17 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)
• Sampling Method: Non-Probability Sample

Study Population

The study will consist of children between the ages of 4-18 and their parents who are being treated at the Oncology Clinic of Altınbaş University Medical Park Bahçelievler Hospital in Istanbul.

You may qualify if:

• Children will be between 4-18 years old
• Communicable children and families
• The child will be hospitalized for inpatient treatment

You may not qualify if:

• Outpatients
• Terminal patients
• Children whose parents cannot be reached will be excluded from work

Sponsors & Collaborators

• Istanbul Gelisim University: lead

Study Sites (1)

Istanbul Gelisim University

Istanbul, Avcılar, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Pain

Interventions

Drug Therapy

Condition Hierarchy (Ancestors)

Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Therapeutics

Study Officials

• Ebru Sevinç

  Arel University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: PROSPECTIVE
• Target Duration: 2 Days
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assistant Professor

Study Record Dates

• First Submitted: May 23, 2024
• First Posted: June 6, 2024
• Study Start: May 1, 2023
• Primary Completion: July 1, 2024
• Study Completion: July 1, 2024
• Last Updated: June 6, 2024

Record last verified: 2024-06

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)