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Personalized Intervention Group (PING): A Proof-of-Concept Study of a Network-Informed, Personalized Approach to Bridging Waiting Times for Psychotherapy

Personalized Intervention Group (PING): A Proof-of-Concept Study of a Network-Informed, Personalized Approach to Bridging Waiting Times for Psychotherapy - PING

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00039177
Enrollment
40
Registered
2026-03-11
Start date
2026-04-14
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

It concerns adolescents who present for outpatient psychotherapy. Following an initial intake session, a suspected diagnosis according to ICD-10 is established. The intervention is delivered transdiagnostically, meaning it is not restricted to a specific disorder category.

Interventions

Group 1: Arm 1: Network-informed modularized personalized group psychotherapy
selection of treatment targets based on person-specific symptom networks
delivery of six modules with personalized content based on the identified treatment targets. Group 2: Arm 2: Initially passive control group, creation of personalized symptom networks and placement on

Sponsors

JGU Mainz
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 17 Years

Inclusion criteria

Inclusion criteria: Inclusion is transdiagnostic, meaning that participants are included regardless of the (suspected) specific disorder, provided that an indication for outpatient psychotherapy has been established during an initial intake session. Additional inclusion criteria are sufficient German language proficiency and written informed consent from the participants and from their legal guardians.

Exclusion criteria

Exclusion criteria: Patients are excluded if they present with acute suicidality or other crisis states requiring immediate treatment, manifest psychotic disorders, or severe intellectual disability, as well as significant cognitive or language impairments that would make participation in the assessments impossible.

Design outcomes

Primary

MeasureTime frame
Primary outcomes are: 1) Level of psychopathological symptoms (general psychopathology, depressive symptoms, anxiety symptoms, aggression), assessed with PSC-D, PHQ-A, SCARED, and RPQ, each measured in both self-report and parent-report; and 2) Change in the individual symptom network, assessed using PECAN-CA in adolescent self-report. Assessment of primary outcomes (pre / post): prior to the start of the group intervention / waiting condition and immediately afterward. For patients who are initially assigned to the waiting condition and later participate in the group intervention, assessments are conducted before and after the waiting period (6–10 weeks) and again after completion of the intervention.

Secondary

MeasureTime frame
At the same assessment time points, child quality of life (KINDL) and illness perceptions (IPQ-R) are assessed via self-report. In addition, therapy progress is assessed using the BFS – Youth Report, and feasibility questions regarding the use of symptom networks are administered after each group session. At post-assessment, an additional feasibility questionnaire on the personalization of the group intervention based on symptom networks is administered.

Countries

Germany

Contacts

Public ContactFelix Vogel

JGU Mainz

fvogel@uni-mainz.de+49 6131 39 32453

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 29, 2026