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Child and Parent-directed Individualized Psychotherapy (CPIP)

Randomized Controlled Trial of Child and Parent-directed Individualized Psychotherapy (CPIP) for Neglected Children With Internalizing Disorders

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05128669
Acronym
AMIS-II-RCT
Enrollment
200
Registered
2021-11-22
Start date
2020-07-21
Completion date
2025-03-20
Last updated
2023-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Child Neglect, Internalizing Disorder

Keywords

emotional/physical neglect, Internalizing disorders, 3 to 8-year old children

Brief summary

With CPIP the investigators opt for a manualized modular psychotherapy designed especially to meet the needs of children with internalizing disorders that suffered or still suffer from emotional or physiological neglect. CPIP helps the child to resolve rigid conflictual internal representations/ working models by individually focusing on caregiver-child interaction, mentalization based interventions with children and caregivers and working with the therapeutic transference relationship with the child and the caregiver. Treatment sessions will take place at CAP. Clinical hypotheses: The main hypothesis of the study is that for children with internalizing disorders and experience of emotional / physical neglect, CPIP & enhanced caregiving support (intervention group) is superior in reducing internalizing symptoms compared to ECS alone (control group). Potential predictors of treatment response, as family context, gender and age, will be examined. Furthermore, the investigators will investigate possible treatment effects and mediating mechanisms, especially changes in DNA methylation profiles, HPA-dysregulation, cognitive-emotional styles, and emotional availability. Additional elements: If the child additionally suffers from traumatic experiences of violence or sexual abuse, elements of Tf-CBT will be applied. Furthermore, elements of Interaction Guidance and ABC including video feedback will be applied in joint caregiver-child sessions. Treatment fidelity: Following the previous study, manualization, careful training and regular supervision will strive to ensure high treatment fidelity which will be systematically assessed in a random sample of two videotaped sessions per family.

Detailed description

Setting: Typically, 25 weekly sessions of approximately 50 minutes; in the clinician's office, family home, or child protection service office (due to the limited compliance expected from some families to attend regular therapeutic sessions). When conducting treatment sessions in the home environment, principles of established and evidence-based home visitation programs, like SafeCare or Nurse-Family Partnership Program will be applied. Therapeutic elements: Reflective developmental guidance, modeling appropriate emotional availability, understanding of the meaning and function of the symptoms within relationships together with the caregivers, identifying and labeling feelings and actions, creation of a neglect narrative (parallel to a trauma narrative) and conflict interpretation together with the child. Three treatment phases: Session 1-5: Building of a working alliance, assessment of family/individual problems and resources, focus formulation; Sessions 6-20: Therapeutic work on the focus; Session 21 to 25: Detachment of the working alliance, summarizing, concluding, fostering future development. Therapeutic strategy: The inner conflict which is currently most pressing and actively determining the child's symptoms as well as jeopardizing mental development in the present will be identified and formulated during the first 5 sessions together with the caregivers and the child (therapeutic focus). The following treatment phase concentrates on the jointly identified problem/conflict that has been aggregated in the focus formulation. The setting will vary (number of parent-only, child-only, and caregiver-child sessions) as a function of whether the focus predominantly lies in the interpersonal (caregiver-child interaction) or intrapersonal realm. Control Condition: Enhanced Caregiving Support (ECS) will serve as the control condition provided by the Allgemeine Sozialdienst (ASD - Community Social Services) of the two participating cities. According to German law (§ 27 SGB VIII), caregivers are entitled to receive caregiving support (CS; Hilfe zur Erziehung) in cases where the child's wellbeing is jeopardized. CS generally includes supportive work across all child-relevant systems (family, neighborhood, (pre-)school, peer group etc.). Appointed social workers and educators provide parenting counseling, family support, and intensive child support according to an individualized helping plan (Hilfeplan). In more severe cases, children are placed in (temporary) day-care centers, children's homes, foster families etc. Within the context of the trial, the investigators will appoint an additional multi-systemic case manager to each case to enhance the quality of case coordination (enhanced CS; ECS). All children and families will receive ECS. the investigators will compare children receiving CPIP plus ECS to children receiving ECS only.

Interventions

PROCEDURECPIP

CPIP is an innovative Child-Parent Individualized Psychotherapy, consisting of 25 sessions, designed by the PI and his clinical collaborators for children with internalizing disorders in the aftermath of childhood neglect. It is informed by Short-term Psychoanalytic Child Therapy, elements of psychoanalytic parent work, videofeedback and Child-Parent Psychotherapy (CPP) and. CPIP supports the child-caregiver relationship and helps the child to resolve rigid conflictual internal representations/working models and improve interpretative and mentalizing techniques.

PROCEDUREECS

Enhanced Caregiving Support (ECS) will serve as the control condition provided by the Allgemeine Sozialdienst (ASD - Community Social Services) of the two participating cities. According to German law (§ 27 SGB VIII), caregivers are entitled to receive caregiving support (CS; Hilfe zur Erziehung) in cases where the child's wellbeing is jeopardized. CS generally includes supportive work across all child-relevant systems (family, neighborhood, (pre-)school, peer group etc.). Appointed social workers and educators provide parenting counseling, family support, and intensive child support according to an individualized helping plan (Hilfeplan). In more severe cases, children are placed in (temporary) day-care centers, children's homes, foster families etc. Within the context of the trial, we will appoint an additional multi-systemic case manager to each case to enhance the quality of case coordination (enhanced CS; ECS). All children and families will receive ECS.

Sponsors

Technische Universität Dresden
CollaboratorOTHER
Medical School Hamburg
CollaboratorOTHER
Technical University of Munich
CollaboratorOTHER
University of Leipzig
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

2 arms, randomized assignment to intervention group (CPIP + ECS) or control group (ECS only), single masked (outcomes assessor), multi-centre trial

Eligibility

Sex/Gender
ALL
Age
3 Years to 8 Years
Healthy volunteers
No

Inclusion criteria

* Inclusion criteria for registration: * Age 3 to 8 * Sufficiently stable psychosocial situation of the child for potential participation in the study * Written informed consent of the patient's parents or legal guardian * Informed oral consent of children (from 6 years) * Release from professional secrecy Teacher / educator * Positive pre-screening for internalizing symptoms * Inclusion criteria for randomisation: * Confirmation that the child's psychosocial situation is sufficiently stable to participate in the study * physical/emotional neglect * DSM-5 internalizing disorder

Exclusion criteria

*

Design outcomes

Primary

MeasureTime frameDescription
Assess superiority of CPIP in addition to Enhanced Caregiving Support (ECS) as compared to ECS alone.The primary efficacy endpoint is taken 13 months after randomisationWe assume superiority of CPIP & ECS compared to ECS alone in reducing internalizing symptoms of participating children. The Child Behavior Checklist 4-18 (CBCL 4-18) - a well-established internationally used questionnaire that reliably and validly captures child internalizing symptoms. The primary efficacy endpoint (pEP) is the CBCL 4-18 internalizing symptoms score (IntS), rated by the primary caregiver at t3 (post-treatment). The scale ranges from 0-62 with higher scores indicating worse outcomes.

Secondary

MeasureTime frameDescription
internalizing symptoms in clinical interviewswithin 4 weeks before randomisation + 7 and 13 months after randomisationIntS for depression and anxiety assessed using the Preschool Age Psychiatric Assessment (PAPA), administered to caregivers by trained Masters-level staff
teacher-rated internalizing symptomswithin 4 weeks before randomisation + 7 and 13 months after randomisation(Nursery-)teacher-rated IntS using Teacher Report Form (TRF 4-18). The scale ranges from 0-70 with higher scores indicating worse outcomes.
secondary caregiver-rated internalizing symptomswithin 4 weeks before randomisation + 7 and 13 months after randomisationSecondary caregiver-rated IntS using Child Behavior Checklist (CBCL 4-18). The scale ranges from 0-62 with higher scores indicating worse outcomes.
Polygenic epigenetic risk scoreswithin 4 weeks before randomisation + 7 months after randomisationchanges in DNA methylation profiles
child-rated internalizing symptomswithin 4 weeks before randomisation + 7 and 13 months after randomisationChild self-reported internalizing symptoms using Berkeley Puppet Interview. The scale ranges from 1-182 with higher scores indicating better outcomes.
Externalizing symptomswithin 4 weeks before randomisation + 7 and 13 months after randomisationExternalizing symptoms (ExtS) rated by caregivers and teachers using the Child Behavior Checklist (CBCL 4-18), Teacher-report Form (TRF) and Berkeley Puppet Interview, respectively. The CBCL ExtS scale ranges from 0-66 with higher scores indicating worse outcomes. The TRF ExtS scale ranges from 0-68 with higher scores indicating worse outcomes.
Adherence to CPIP interventions7 months after randomisationnumber of sessions attended by primary caregiver and by child for secondary/sensitivity analyses
caregiver-rated internalizing symptoms for mid/long-term effects13 months after randomisationCaregiver-rated IntS using Child Behavior Checklist (CBCL 4-18) at t4 to assess mid/long-term effects. The scale ranges from 0-62 with higher scores indicating worse outcomes.
Feasibility-related endpoints - Acceptability of CPIP rated by children7 months after randomisationAcceptability of CPIP rated by children: Items derived from the German version of Therapeutic Alliance Scales for Children (TASC)
Feasibility-related endpoints - Acceptability of CPIP rated by therapists7 months after randomisationAcceptability of CPIP rated by caregivers/ parents using Treatment evaluation questionnaire (Fragebogen zur Beurteilung der Behandlung - FBB)
Cognitive-emotional style/mentalizing capacitywithin 4 weeks before randomisation + 7 months after randomisationIn an exploratory fashion, the investigators will test whether the child's ability to mentalize improve after the intervention and whether improvement in this ability is a mediator of the treatment effect. Child's ability to mentalize assessed by the Process Scales (Hill et al., 2009) and the MacArthur Narrative Coding Manual (MNCM; Robsinson et al., 2002) using the indices for narrative coherence (range: 1-12), intentionality (range: 1-12), with higher scores indicating better outcome.
Quality of the parent-child interaction (EAS)within 4 weeks before randomisation + 7 months after randomisationIn an exploratory fashion, the investigators will test whether the quality of parent-child interaction improve after the intervention and whether this improvement in interaction quality is a mediator of the treatment effect. Quality of the parent-child interaction assessed by the Emotional Availability Scales (EAS), specifically four caregiver scales (1. sensitivity, 2. structuring, 3. nonintrusiveness, and 4. nonhostility) and two child scales (1.responsiveness to mother and 2. involvement of mother). Codes on the scales range from 1 to 7, with higher scores indicating better outcome.
Cortisol secretionwithin 4 weeks before randomisation + 3.5 months after randomisation + 7 and 13 months after randomisationhair cortisol concentrations (HCC) in the first 3 cm scalp hair segment at posterior vertex (\ cumulative secretion over last 3 months)
Feasibility-related endpoints - CPIP retention rates7 months after randomisationAcceptability of CPIP - retention rates. We expect a high rate of retention until end of the intervention.
Feasibility-related endpoints - Adherence to CPIP interventions7 months after randomisationAdherence to CPIP interventions: coding of session videos using a Q-sort rating
Feasibility-related endpoints - Acceptability of CPIP rated by caregivers/ parents7 months after randomisationAcceptability of CPIP rated by caregivers/ parents using Treatment evaluation questionnaire (Fragebogen zur Beurteilung der Behandlung - FBB)

Countries

Germany

Contacts

Primary ContactLars Otto White, Dr. phil
LarsOtto.White@medizin.uni-leipzig.de+49 (0) 341 - 9724018

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026