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KOPPeling: Help From Your Own Circle

Primary Purpose

Children of Parents With a Mental Illness (COPMI)

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
KOPPeling
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Children of Parents With a Mental Illness (COPMI) focused on measuring COPMI, Prevention, Social participation, Mental illness

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: The family has children aged 0-18 living at home The parental disorder influences the parent's (or parents') ability to carry out several important parental tasks, placing their offspring at risk of taking over these tasks Exclusion Criteria: - The family has no existing social network

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Other

    Arm Label

    Intervention (KOPPeling)

    Waiting list

    Arm Description

    In this arm participants directly receive the KOPPeling intervention.

    In this arm participants are placed on a waiting list (ten to twelve weeks) before receiving the KOPPeling intervention.

    Outcomes

    Primary Outcome Measures

    Change in Quality of Life (QoL) of COPMI
    QoL of COPMI, which will be assessed with the KIDSCREEN-27. The KIDSCREEN-27 includes 27 items measuring five dimensions of QoL on a Rasch scale including: 1) physical well-being, 2) psychological well-being, 3) autonomy and parent relation, 4) peers and social support, and 5) school environments. Each item is measured on a five-point Likert scale. Some items are negatively formulated through which the item scores need to be reversed. The overall score is calculated by summing up all the items. Therefore, higher scores indicate higher QoL.

    Secondary Outcome Measures

    Change in mental health of COPMI
    The mental health of COPMI, which will be assessed with the Strengths and Difficulties Questionnaire (SDQ). The SDQ consists out of 25 items (five scales of five items each) including the following subscales: 1) emotional symptoms, 2) conduct problems, 3) hyperactivity/inattention, 4) peer relationships problem and 5) prosocial behaviour. Each attribute is scored on a zero to ten scale. While a score of 0 is the best outcome concerning the emotional, conduct, hyperactivity, and peer relationship scale (adding up to a 0 to 40 scale), a score of 10 is the best outcome concerning the pro-social behaviour scale.
    Change in parental stress of COPMI parents
    The parental stress of COPMI parents, which will be assessed with the Nijmeegse Ouderlijke Stress Index (NOSI-K). The NOSI-K includes 25-items assessing parental perceived difficulty in child rearing. Each item, which states a parental-stress-related statement, is rated on a five-point Likert scale ranging from 1 (totally disagree) to (totally agree).
    Change in engagement in outdoor activities of COPMI
    The engagement in outdoor activities will be measured in an ecological momentary assessment.
    Change in guilt of COPMI when engaging in outdoor activities
    The associated guilt of engaging in outdoor activities of COPMI will be assessed in an ecological momentary assessment in which the Guilt and Shame Questionnaire for Adolescents of Parents with a Mental Illness (GSQ-APMI) will be used. The GSQ-APMI includes 10 items. Five items were developed to measure shame and five items to measure guilt. A total score is not applicable as the GSQ-APMI results in two scores: one reflecting feelings of guilt and one reflecting feelings of shame. Higher scores reflect greater feelings of guilt or shame.
    Experiences of the social networks made with KOPPeling
    The experiences of the social network with KOPPeling, which will be assessed in a qualitative interview with a purposive sample taken from the social networks of included families.
    Promoting and hindering factors of making KOPPeling a widely applicable intervention
    The promoting and hindering factors for making the intervention widely applicable, which will be assessed with the Measuring Instrument for Determinants of Innovations (MIDI).

    Full Information

    First Posted
    February 21, 2023
    Last Updated
    June 13, 2023
    Sponsor
    University Medical Center Groningen
    Collaborators
    Accare, WIJ Groningen, GGZ Friesland, Amaryllis Leeuwarden, Hanzehogeschool Groningen
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05829408
    Brief Title
    KOPPeling: Help From Your Own Circle
    Official Title
    KOPPeling: Help From Your Own Circle
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2023 (Anticipated)
    Primary Completion Date
    August 31, 2026 (Anticipated)
    Study Completion Date
    August 31, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University Medical Center Groningen
    Collaborators
    Accare, WIJ Groningen, GGZ Friesland, Amaryllis Leeuwarden, Hanzehogeschool Groningen

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The goal of this randomized clinical trial is to test the effectiveness of the KOPPeling intervention that aims at unburdening COPMI (Children Of Parents with a Mental Illness). COPMI are at risk of overtaking the tasks of their parents when their parents are unable to fulfil such due to their psychiatric condition. By overtaking tasks and the urge to always take care of their parents, COPMI often do not participate in outdoor activities, which are necessary for their socio-emotional development. Moreover, insufficient socio-emotional development and parentification are risk factors for the development of psychiatric conditions. KOPPeling is an intervention for COPMI families that focuses on activating the social networks of the families. Within KOPPeling, a strategic plan will be developed and carried out with the goal of receiving support from the social network that will overtake tasks of the family to unburden COPMI. This study aims to answer the following questions: To what extent does KOPPeling lead to an increase in Quality of Life (QoL) among COPMI? To what extent does KOPPeling lead to an increase in mental health among COPMI? To what extent does KOPPeling lead to a reduction of parenting stress among COPMI parents? To what extent does KOPPeling lead to an increase in outdoor activities among COPMI? How does KOPPeling affect the feelings of guilt of COPMI when engaging in outdoor activities? What pre-conditions are needed to make KOPPeling widely applicable? What are the long-term effects of KOPPeling on the QoL and psychological problems among COPMI and parental stress among COPMI parents? Participants will participate in the ten-to-twelve-week long KOPPeling intervention. Researchers will compare the intervention group with a waiting list control group to test the effect of KOPPeling on the QoL and mental health of COPMI and parental stress of parents.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Children of Parents With a Mental Illness (COPMI)
    Keywords
    COPMI, Prevention, Social participation, Mental illness

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    128 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention (KOPPeling)
    Arm Type
    Other
    Arm Description
    In this arm participants directly receive the KOPPeling intervention.
    Arm Title
    Waiting list
    Arm Type
    Other
    Arm Description
    In this arm participants are placed on a waiting list (ten to twelve weeks) before receiving the KOPPeling intervention.
    Intervention Type
    Behavioral
    Intervention Name(s)
    KOPPeling
    Intervention Description
    KOPPeling lasts ten to twelve weeks and will be administered by health care professionals.
    Primary Outcome Measure Information:
    Title
    Change in Quality of Life (QoL) of COPMI
    Description
    QoL of COPMI, which will be assessed with the KIDSCREEN-27. The KIDSCREEN-27 includes 27 items measuring five dimensions of QoL on a Rasch scale including: 1) physical well-being, 2) psychological well-being, 3) autonomy and parent relation, 4) peers and social support, and 5) school environments. Each item is measured on a five-point Likert scale. Some items are negatively formulated through which the item scores need to be reversed. The overall score is calculated by summing up all the items. Therefore, higher scores indicate higher QoL.
    Time Frame
    At T0 (baseline, start of intervention), T1 (end of intervention) and T2 (three months after the end of intervention), total time frame: 22 to 24 weeks
    Secondary Outcome Measure Information:
    Title
    Change in mental health of COPMI
    Description
    The mental health of COPMI, which will be assessed with the Strengths and Difficulties Questionnaire (SDQ). The SDQ consists out of 25 items (five scales of five items each) including the following subscales: 1) emotional symptoms, 2) conduct problems, 3) hyperactivity/inattention, 4) peer relationships problem and 5) prosocial behaviour. Each attribute is scored on a zero to ten scale. While a score of 0 is the best outcome concerning the emotional, conduct, hyperactivity, and peer relationship scale (adding up to a 0 to 40 scale), a score of 10 is the best outcome concerning the pro-social behaviour scale.
    Time Frame
    At T0 (baseline, start of intervention), T1 (end of intervention) and T2 (three months after the end of intervention), total time frame: 22 to 24 weeks
    Title
    Change in parental stress of COPMI parents
    Description
    The parental stress of COPMI parents, which will be assessed with the Nijmeegse Ouderlijke Stress Index (NOSI-K). The NOSI-K includes 25-items assessing parental perceived difficulty in child rearing. Each item, which states a parental-stress-related statement, is rated on a five-point Likert scale ranging from 1 (totally disagree) to (totally agree).
    Time Frame
    At T0 (baseline, start of intervention), T1 (end of intervention) and T2 (three months after the end of intervention), total time frame: 22 to 24 weeks
    Title
    Change in engagement in outdoor activities of COPMI
    Description
    The engagement in outdoor activities will be measured in an ecological momentary assessment.
    Time Frame
    For one week after the start of the intervention and one week before the end of the intervention
    Title
    Change in guilt of COPMI when engaging in outdoor activities
    Description
    The associated guilt of engaging in outdoor activities of COPMI will be assessed in an ecological momentary assessment in which the Guilt and Shame Questionnaire for Adolescents of Parents with a Mental Illness (GSQ-APMI) will be used. The GSQ-APMI includes 10 items. Five items were developed to measure shame and five items to measure guilt. A total score is not applicable as the GSQ-APMI results in two scores: one reflecting feelings of guilt and one reflecting feelings of shame. Higher scores reflect greater feelings of guilt or shame.
    Time Frame
    For one week after the start of the intervention and one week before the end of the intervention
    Title
    Experiences of the social networks made with KOPPeling
    Description
    The experiences of the social network with KOPPeling, which will be assessed in a qualitative interview with a purposive sample taken from the social networks of included families.
    Time Frame
    At the end of the intervention (ten to twelve weeks after the start of the intervention)
    Title
    Promoting and hindering factors of making KOPPeling a widely applicable intervention
    Description
    The promoting and hindering factors for making the intervention widely applicable, which will be assessed with the Measuring Instrument for Determinants of Innovations (MIDI).
    Time Frame
    At the end of the intervention (ten to twelve weeks after the start of the intervention)

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: The family has children aged 0-18 living at home The parental disorder influences the parent's (or parents') ability to carry out several important parental tasks, placing their offspring at risk of taking over these tasks Exclusion Criteria: - The family has no existing social network
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Lisa Maeder, M.Sc.
    Phone
    +31681504012
    Email
    l.maeder@umcg.nl
    First Name & Middle Initial & Last Name or Official Title & Degree
    Frederike Jörg, Dr.
    Email
    f.jorg@umcg.nl
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Frederike Jörg, Dr.
    Organizational Affiliation
    University Medical Center Groningen
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    19807604
    Citation
    Ravens-Sieberer U, Gosch A, Rajmil L, Erhart M, Bruil J, Duer W, Auquier P, Power M, Abel T, Czemy L, Mazur J, Czimbalmos A, Tountas Y, Hagquist C, Kilroe J, Kidscreen Group E. KIDSCREEN-52 quality-of-life measure for children and adolescents. Expert Rev Pharmacoecon Outcomes Res. 2005 Jun;5(3):353-64. doi: 10.1586/14737167.5.3.353.
    Results Reference
    background
    PubMed Identifier
    12601558
    Citation
    Muris P, Meesters C, van den Berg F. The Strengths and Difficulties Questionnaire (SDQ)--further evidence for its reliability and validity in a community sample of Dutch children and adolescents. Eur Child Adolesc Psychiatry. 2003 Jan;12(1):1-8. doi: 10.1007/s00787-003-0298-2.
    Results Reference
    background
    PubMed Identifier
    14689260
    Citation
    van Widenfelt BM, Goedhart AW, Treffers PD, Goodman R. Dutch version of the Strengths and Difficulties Questionnaire (SDQ). Eur Child Adolesc Psychiatry. 2003 Dec;12(6):281-9. doi: 10.1007/s00787-003-0341-3.
    Results Reference
    background
    PubMed Identifier
    18509902
    Citation
    Shiffman S, Stone AA, Hufford MR. Ecological momentary assessment. Annu Rev Clin Psychol. 2008;4:1-32. doi: 10.1146/annurev.clinpsy.3.022806.091415.
    Results Reference
    background
    PubMed Identifier
    24951511
    Citation
    Fleuren MA, Paulussen TG, Van Dommelen P, Van Buuren S. Towards a measurement instrument for determinants of innovations. Int J Qual Health Care. 2014 Oct;26(5):501-10. doi: 10.1093/intqhc/mzu060. Epub 2014 Jun 20.
    Results Reference
    background

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