CClinicalTrials.gg
CompletedNCT04474678Updated Jan 9, 2024

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

An interventional study of "My Logbook! - I know my way around!" in Brain Tumor, Neurofibromatoses and Sarcoma, sponsored by Medical University of Vienna. Completed at 22 sites in 4 countries. Open to participants aged 6 Years to 14 Years. Per ClinicalTrials.gov, last updated 2024-01-09.

Sponsored by Medical University of Vienna · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
240
Allocation
Not applicable
Ages
6 Years to 14 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Brain Tumor
  • Neurofibromatoses
  • Sarcoma
  • Leukemia
  • Hematologic Diseases
  • Neuroblastoma
03

In context

Neuroblastoma

625 studies on the registry are indexed under Neuroblastoma; 122 are open to participants now.

This study's enrollment of 240 is above the median of 32 across 475 interventional studies indexed under Neuroblastoma.

Browse Neuroblastoma studies →

Lead sponsor

Medical University of Vienna is the lead sponsor of 1,076 studies on the registry; 177 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 14 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
240 participants (actual)

Study arms

  • Other
    All Patients

    Since this is a single-group study, all patients are within the same arm

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

Interventions

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

    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.

06

What researchers measure

Primary outcomes

  1. Emotional well-being, T1

    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.

    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

  2. Emotional well-being, T2

    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.

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

  3. Emotional well-being, T3

    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.

    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

  4. Emotional well-being, T4

    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.

    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

  5. Emotional well-being, T5

    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.

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

  6. Knowledgeability, T1

    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.

    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

  7. Knowledgeability, T2

    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.

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

  8. Knowledgeability, T3

    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.

    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

  9. Knowledgeability, T4

    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.

    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

  10. Knowledgeability, T5

    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.

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

  11. Feasibility of program

    Rating of feasibility of the program by medical staff

    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

Secondary outcomes

  1. Intelligence test

    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

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

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

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

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

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

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

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

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

    Questionnaire for the assessment of health competence in children and adolescents

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

  5. Medical information

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

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

  6. Demographic data

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

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

07

Study locations

22 sites
  • Kepler Universitätsklinikum
    Linz, Oberösterreich 4021, Austria
  • Rehabilitationszentrum St. Veit im Pongau
    St. Veit, Salzburg 5621, Austria
  • Medical University Graz
    Graz, Austria
  • Medical University of Vienna
    Vienna, 1090, Austria
  • St. Anna Kinderspital
    Vienna, 1090, Austria
  • Universitätsklinikum Frankfurt am Main
    Frankfurt am Main, Hessen 60590, Germany
  • Medizinische Hochschule Hannover
    Hannover, Niedersachsen 30625, Germany
  • Universitätsklinikum Essen
    Essen, Nordrhein-Westfalen 45147, Germany
  • Universitätsklinikum Münster
    Münster, Nordrhein-Westfalen 48149, Germany
  • Universitätsklinikum des Saarlandes
    Homburg, Saarland 66421, Germany
  • Universitätsklinikum Leipzig
    Leipzig, Sachsen 04103, Germany
  • Klinik Bad Oexen
    Bad Oeynhausen, 32549, Germany
  • Charité - Universitätsmedizin Berlin
    Berlin, Germany
  • Luca-Dethlefsen-Hilfe e.V.
    Bielefeld, Germany
  • Universitätsklinikum Carl Gustav Carus Dresden
    Dresden, Germany
  • Universitätsklinikum Hamburg-Eppendorf
    Hamburg, Germany
  • Universitätsklinikum Mannheim
    Mannheim, Germany
  • Universitätsklinikum Regensburg
    Regensburg, Germany
  • Universitätsklinikum Tübingen
    Tübingen, Germany
  • Universitätsklinikum Würzburg
    Würzburg, Germany
  • Ospedale di Bolzano
    Bolzano, Trentino-Alto Adige 39100, Italy
  • Inselspital, Universitätsspital Bern
    Bern, Switzerland
08

References and documents

Publications

  • Kazak AE, Abrams AN, Banks J, Christofferson J, DiDonato S, Grootenhuis MA, Kabour M, Madan-Swain A, Patel SK, Zadeh S, Kupst MJ. Psychosocial Assessment as a Standard of Care in Pediatric Cancer. Pediatr Blood Cancer. 2015 Dec;62 Suppl 5:S426-59. doi: 10.1002/pbc.25730. PubMed 26700916 ↗
  • Scialla MA, Canter KS, Chen FF, Kolb EA, Sandler E, Wiener L, Kazak AE. Delivery of care consistent with the psychosocial standards in pediatric cancer: Current practices in the United States. Pediatr Blood Cancer. 2018 Mar;65(3):10.1002/pbc.26869. doi: 10.1002/pbc.26869. Epub 2017 Oct 28. PubMed 29080381 ↗
  • Baxter S, Johnson M, Chambers D, Sutton A, Goyder E, Booth A. The effects of integrated care: a systematic review of UK and international evidence. BMC Health Serv Res. 2018 May 10;18(1):350. doi: 10.1186/s12913-018-3161-3. PubMed 29747651 ↗
  • Schurman JV, Gayes LA, Slosky L, Hunter ME, Pino FA. Publishing quality improvement work in Clinical Practice in Pediatric Psychology: The "why" and "how to". Clinical Practice in Pediatric Psychology. 2015 Mar; 3(1):80.
  • Schröder HM, Lilienthal S, Schreiber-Gollwitzer BM, Griessmeier B, Leiss U. Psychosoziale Versorgung in der Pädiatrischen Onkologie und Hämatologie. PSAPOH (Hg.). 2013.
  • Stuber ML, Meeske KA, Krull KR, Leisenring W, Stratton K, Kazak AE, Huber M, Zebrack B, Uijtdehaage SH, Mertens AC, Robison LL, Zeltzer LK. Prevalence and predictors of posttraumatic stress disorder in adult survivors of childhood cancer. Pediatrics. 2010 May;125(5):e1124-34. doi: 10.1542/peds.2009-2308. PubMed 20435702 ↗
  • Koch U, Mehnert A, Harter M. [Chronic somatic disorders and psychological comorbidity]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2011 Jan;54(1):1-3. doi: 10.1007/s00103-010-1196-7. No abstract available. German. PubMed 21246321 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04474678
Lead sponsor
Medical University of Vienna
Collaborators
St. Anna Kinderspital, Austria, Charite University, Berlin, Germany, Cnopfsche Kinderklinik, Nürnberg, Kepler University Hospital, University Hospital, Saarland, Hannover Medical School, Krankenhaus Bozen, Goethe University, Universitätsklinikum Hamburg-Eppendorf, Universitätsklinikum Leipzig, University Hospital Muenster, University Hospital Tuebingen, Salzburger Landeskliniken, Leuwaldhof St.Veit (Kinder- und Jugendreha), University Hospital, Essen, Medical University of Graz, University Hospital Erlangen, Wuerzburg University Hospital, Klinik Bad Oexen, Germany, Universitätsklinikum Köln, University Hospital Schleswig-Holstein, University Hospital Carl Gustav Carus, Universitätsmedizin Mannheim, University Hospital Regensburg, Luca-Dethlefsen-Hilfe e.V., Insel Gruppe AG, University Hospital Bern, Staedtisches Klinikum Karlsruhe
Responsible party
Dr. Liesa J. Weiler-Wichtl (Project Coordinator, Medical University of Vienna) — Principal investigator
First posted
Jul 17, 2020
Start date
Sep 7, 2020
Primary completion
Dec 31, 2023
Completion
Dec 31, 2023
Last update
Jan 9, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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