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

Sponsor
Medical University of Vienna (Other)
Overall Status
Recruiting
CT.gov ID
NCT04474678
Collaborator
St. Anna Kinderspital, Austria (Other), Charite University, Berlin, Germany (Other), Cnopfsche Kinderklinik, Nürnberg (Other), Kepler University Hospital (Other), University Hospital, Saarland (Other), Hannover Medical School (Other), Krankenhaus Bozen (Other), University Hospital Frankfurt (Other), Universitätsklinikum Hamburg-Eppendorf (Other), Universitätsklinikum Leipzig (Other), University Hospital Muenster (Other), University Hospital Tuebingen (Other), Salzburger Landeskliniken (Other), Leuwaldhof St.Veit (Kinder- und Jugendreha) (Other), University Hospital, Essen (Other), Medical University of Graz (Other), University Hospital Erlangen (Other), Wuerzburg University Hospital (Other), Klinik Bad Oexen, Germany (Other), Universitätsklinikum Köln (Other), University Hospital Schleswig-Holstein (Other), University Hospital Carl Gustav Carus (Other), Universitätsmedizin Mannheim (Other), University Hospital Regensburg (Other), Luca-Dethlefsen-Hilfe e.V. (Other), University Hospital Inselspital, Berne (Other)
128
27
1
23.8
4.7
0.2

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: "My Logbook! - I know my way around!"
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
128 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official 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.
Actual Study Start Date :
Sep 7, 2020
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
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!"
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.

Outcome Measures

Primary Outcome Measures

  1. Emotional well-being, T1 [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 [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 [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 [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 [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 [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 [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 [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 [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 [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 [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 Outcome Measures

  1. Intelligence test [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) [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) [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) [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 [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 [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

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 14 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kepler Universitätsklinikum Linz Oberösterreich Austria 4021
2 Rehabilitationszentrum St. Veit im Pongau St. Veit Salzburg Austria 5621
3 Medical University Graz Graz Austria
4 Uniklinikum Salzburg Salzburg Austria 5020
5 Medical University of Vienna Vienna Austria 1090
6 St. Anna Kinderspital Vienna Austria 1090
7 Cnopfsche Kinderklinik Nürnberg Bayern Germany 90419
8 Universitätsklinikum Frankfurt am Main Frankfurt am Main Hessen Germany 60590
9 Medizinische Hochschule Hannover Hannover Niedersachsen Germany 30625
10 Universitätsklinikum Essen Essen Nordrhein-Westfalen Germany 45147
11 Universitätsklinikum Münster Münster Nordrhein-Westfalen Germany 48149
12 Universitätsklinikum des Saarlandes Homburg Saarland Germany 66421
13 Universitätsklinikum Leipzig Leipzig Sachsen Germany 04103
14 Klinik Bad Oexen Bad Oeynhausen Germany 32549
15 Charité - Universitätsmedizin Berlin Berlin Germany
16 Luca-Dethlefsen-Hilfe e.V. Bielefeld Germany
17 Uniklinik Köln Cologne Germany
18 Universitätsklinikum Carl Gustav Carus Dresden Dresden Germany
19 Universitätsklinikum Erlangen Erlangen Germany
20 Universitätsklinikum Hamburg-Eppendorf Hamburg Germany
21 Universitätsklinikum Schleswig-Holstein Kiel Germany
22 Universitätsklinikum Mannheim Mannheim Germany
23 Universitätsklinikum Regensburg Regensburg Germany
24 Universitätsklinikum Tübingen Tübingen Germany
25 Universitätsklinikum Würzburg Würzburg Germany
26 Ospedale di Bolzano Bolzano Trentino-Alto Adige Italy 39100
27 Inselspital, Universitätsspital Bern Bern Switzerland

Sponsors and Collaborators

  • Medical University of Vienna
  • St. Anna Kinderspital, Austria
  • Charite University, Berlin, Germany
  • Cnopfsche Kinderklinik, Nürnberg
  • Kepler University Hospital
  • University Hospital, Saarland
  • Hannover Medical School
  • Krankenhaus Bozen
  • University Hospital Frankfurt
  • 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.
  • University Hospital Inselspital, Berne

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Liesa J. Weiler-Wichtl, Project Coordinator, Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT04474678
Other Study ID Numbers:
  • 1564/2017
First Posted:
Jul 17, 2020
Last Update Posted:
Feb 23, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 23, 2022