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Completed

NCT Number: NCT04474678

Quality Improvement Project - "My Logbook! - I Know my Way Around!"; ("Mein Logbuch - Ich Kenne Mich Aus!")

In this study, the main goal is to implement and evaluate a novel, evidence-based psycho-educative program for children in oncological care. Patients are provided with booklets tailored to each specific stage of their treatment. Among other factors, children's emotional well-being is evaluated as well as feasibility. The study is carried out at multiple sites across Austria, Germany and Italy/South Tirol.

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Key information

About this study

It is well documented that the prevalence of mental disorders in childhood cancer survivors is twice to quadruple compared to healthy controls. Effects range from impaired emotional balance, fear of recidivisms, helplessness, depression to post traumatic stress disorder.

As a basis for interventions to preventively address these issues and moreover, to achieve defined psychosocial goals in the field of paediatric oncology, guidelines and standards systematically describe stressors and resources in particularly challenging situations. Nevertheless, despite these guidelines, actual care is quite heterogenous due to differences in setting, provision and profession. Studies show that integrated models of psychosocial care yield better outcomes. Integrated care systems can enhance patient satisfaction, increase perceived quality of care, and enable access to services and reduce service costs. Highly complex, system-wide interventions such as models of integrated care represent considerable challenges for operationalisation of relevant factors and evaluation of whole processes compared to single interventions (e.g. relaxation techniques). Quality improvement (QI) is an iterative process designed to make controlled changes within the health care delivery system to provide patients with high-quality care that meets both their expectations and needs. In terms of quality assurance, this QI Project aims to operationalize recommendations of the S3 guideline for psychosocial care which results in a combined process- and patient-oriented intervention and evaluation tool - bridging the gap between standards/evidence and clinical practice.

The "Onco-Mini-Version" of "My Logbook - I know my way around" already comprises a Starter-Kit and 8 booklets, which cover at least one main issue of every treatment phase: initial contact, medical assessment (MRI), supportive therapy (chemotherapy, radio therapy), rehabilitation and after-care. All interventions are carried out by a clinical psychologist or psychosocial staff specialized in pediatric psychooncology and are understood as part of an integrated care system. Every booklet provides practical materials with enhanced stimulating elements to encourage the child to explore actively. The booklets are structured in two face-to-face sessions covering psychoeducational, activity & practice and reflective aspects.

The core of this QI project is a multilevel and interdisciplinary approach characterized by iterative processes. PDSA (Plan, Do, Study, Act) cycles were applied in all steps of conceptualization and implementation of this project. It aims to systematically improve psychosocial care of pediatric cancer patients through being implemented in a large number of hospitals in the German-speaking world. The proposed multicenter pilot phase promotes emotional well-being and level of information of the child during treatment through transfer of knowledge and coping skills. Moreover, it addresses feasibility of the tool but also the impact of medical procedures on feasibility. In the long term, the program is intended to help attenuate psychological late effects of oncological conditions and their treatments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

experimental group:

  • currently or formerly treated for oncological condition
  • children/families at standard risk (Pediatric Psychosocial Preventative Health Model (PPPHM))
  • at least average cognitive abilities (as measured via intelligence test)

Inclusion criteria

control group:

  • currently or formerly treated for oncological condition

Exclusion criteria

  • non-German speaking
  • Major vision impairments
  • Major auditive impairments

Treatment and study plan

"My Logbook! - I know my way around!"

Other

Special issues/booklets of "My Logbook - I know my way around!" - Every booklet is based on evidence-based interventions. It illustrates psychosocial and interdisciplinary processes in a standardized way, resulting in a practical guide ("My Logbook") to accompany the child throughout all stages of oncological treatment.

Primary outcomes

  1. Emotional well-being, T1

    Time frame: Based on the medical therapy protocol, after medical consultation, prior to first session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients' emotional well-being is evaluated using a visual array of emotional displays. Patients can choose three emotions that describe their current situation best. For analysis, emotions are categorized into positive, neutral, and negative emotions. Emotional well-being is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house, publication is pending.

  2. Emotional well-being, T2

    Time frame: Post to first session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients' emotional well-being is evaluated using a visual array of emotional displays. Patients can choose three emotions that describe their current situation best. For analysis, emotions are categorized into positive, neutral, and negative emotions. Emotional well-being is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house, publication is pending.

  3. Emotional well-being, T3

    Time frame: During, but before completion of treatment; prior to second session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients' emotional well-being is evaluated using a visual array of emotional displays. Patients can choose three emotions that describe their current situation best. For analysis, emotions are categorized into positive, neutral, and negative emotions. Emotional well-being is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house, publication is pending.

  4. Emotional well-being, T4

    Time frame: During, post to second session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients' emotional well-being is evaluated using a visual array of emotional displays. Patients can choose three emotions that describe their current situation best. For analysis, emotions are categorized into positive, neutral, and negative emotions. Emotional well-being is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house, publication is pending.

  5. Emotional well-being, T5

    Time frame: During, but before completion of treatment - through study completion or end of medical treatment, an average of 1 year

    Patients' emotional well-being is evaluated using a visual array of emotional displays. Patients can choose three emotions that describe their current situation best. For analysis, emotions are categorized into positive, neutral, and negative emotions. Emotional well-being is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house, publication is pending.

  6. Knowledgeability, T1

    Time frame: Based on the medical therapy protocol, after medical consultation, prior to first session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients are asked to rate their own knowledgeability regarding treatment, illness and hospital environment on a five-point scale ranging from "beginner" to "expert". Knowledgeability is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house.

  7. Knowledgeability, T2

    Time frame: Post to first session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients are asked to rate their own knowledgeability regarding treatment, illness and hospital environment on a five-point scale ranging from "beginner" to "expert". Knowledgeability is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house.

  8. Knowledgeability, T3

    Time frame: During, but before completion of treatment; prior to second session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients are asked to rate their own knowledgeability regarding treatment, illness and hospital environment on a five-point scale ranging from "beginner" to "expert". Knowledgeability is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house.

  9. Knowledgeability, T4

    Time frame: During, post to second session of the special issue (booklet) - through study completion or end of medical treatment, an average of 1 year

    Patients are asked to rate their own knowledgeability regarding treatment, illness and hospital environment on a five-point scale ranging from "beginner" to "expert". Knowledgeability is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house.

  10. Knowledgeability, T5

    Time frame: During, but before completion of treatment - through study completion or end of medical treatment, an average of 1 year

    Patients are asked to rate their own knowledgeability regarding treatment, illness and hospital environment on a five-point scale ranging from "beginner" to "expert". Knowledgeability is evaluated longitudinally over multiple points of time. The diagnostic tool was developed in-house.

  11. Feasibility of program

    Time frame: Feasibility of program is evaluated following the second session which on average takes place one to six months after start of the treatment of the special issue (booklet). - through study completion or end of medical treatment, an average of 1 year

    Rating of feasibility of the program by medical staff

Secondary outcomes

  1. Intelligence test

    Time frame: During the first two months from diagnosis or start of psychosocial treatment - up to three Months

    Patients are administered a standardized intelligence test, dependent on their age, e.g.

    Wechsler Intelligence Scale for Children IV WISC-IV, Petermann & Petermann, 2014 or other comparable methods due to clinical standards

  2. Strengths and Difficulties Questionnaire (SDQ; Goodman, 1999)

    Time frame: During the first two months from diagnosis or start of psychosocial treatment - up to three Months

    The Strengths and Difficulties Questionnaire (SDQ) is a brief behavioural screening questionnaire about 3-16 year olds.

  3. KINDLR (Ravens-Sieberer & Bullinger, 2000)

    Time frame: During the first two months from diagnosis or start of psychosocial treatment - up to three Months

    The KINDLR is a standardized questionnaire for the assessment of quality of life in children and adolescents.

  4. Questionnaire on Health Competence in Children and Adolescents, (Weiler, Fohn, Pletschko, Schwarzinger, & Leiss, 2017)

    Time frame: During the first two months from diagnosis or start of psychosocial treatment - up to three Months

    Questionnaire for the assessment of health competence in children and adolescents

  5. Medical information

    Time frame: Within the first week of treatment - up to three Months

    Diagnosis, date of diagnosis, pre-existing conditions, secondary conditions, form of treatment/therapy, psychiatric diagnoses, neurological status

  6. Demographic data

    Time frame: During the first two months from diagnosis or start of psychosocial treatment - up to three Months

    Age of patient, sex, parents' education, parents' profession, school form, mother language of patient

Sponsors and collaborators

Lead sponsor

Medical University of Vienna

Other

Collaborators

  • Charite University, Berlin, Germany
  • Cnopfsche Kinderklinik, Nürnberg
  • Goethe University
  • Hannover Medical School
  • Insel Gruppe AG, University Hospital Bern
  • Kepler University Hospital
  • Klinik Bad Oexen, Germany
  • Krankenhaus Bozen
  • Leuwaldhof St.Veit (Kinder- und Jugendreha)
  • Luca-Dethlefsen-Hilfe e.V.
  • Medical University of Graz
  • Salzburger Landeskliniken
  • St. Anna Kinderspital, Austria
  • Staedtisches Klinikum Karlsruhe
  • University Hospital Carl Gustav Carus
  • University Hospital Erlangen
  • University Hospital Muenster
  • University Hospital Regensburg
  • University Hospital Schleswig-Holstein
  • University Hospital Tuebingen
  • University Hospital, Essen
  • University Hospital, Saarland
  • Universitätsklinikum Hamburg-Eppendorf
  • Universitätsklinikum Köln
  • Universitätsklinikum Leipzig
  • Universitätsmedizin Mannheim
  • Wuerzburg University Hospital

Registry information

Official study title

A Quality Improvement Project to Implement Psychosocial Care Standards in Clinical Practice in Pediatric Oncology "My Logbook! - I Know my Way Around!" ("Mein Logbuch - Ich Kenne Mich Aus!") Development and Evaluation of a Consensus and Evidence Based Psychosocial Therapy Tool in a Preliminary Psychosocial Study on Therapy Optimization.

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Jul 17, 2020
Registry last updated
Jan 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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