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Patient perspective on a novel music therapy intervention for songwriting: acceptability and feasibility.

Patient perspective on a novel music therapy intervention for songwriting: acceptability and feasibility.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00031153
Enrollment
35
Registered
2023-01-26
Start date
2023-02-21
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

F32 F60.3 F33

Interventions

Group 1: Interventional = TS, 16 sessions (each 90 min), 2x per week (intervention period 8 weeks). Each session is structured in the same way. The participant goes individually each time in a group o

Sponsors

Universitätsklinikum Hamburg-Eppendorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: Presence of ICD - 11 (clinician diagnosis) emotional-instable personality disorder. Presence of a depressive disorder according to ICD - 11 Gender: male, female, diverse Minimum age: 18 Maximum age: 25 Consent to participate Ability to give consent Sufficient understanding of the German language Group ability

Exclusion criteria

Exclusion criteria: Medical contraindication to participation in group music therapy: acute suicidal tendency, acute psychotic experience, pronounced dissociative experience, no existing group ability, tendency to acoustic stimulus overload.

Design outcomes

Primary

MeasureTime frame
Subjective evaluation of group music therapy Therapeutic Songwriting (TR) at time T1: The subjective evaluation questionnaire captures patients' opinions of TS and subjective symptom improvement. After each session, participants will receive a post-session questionnaire (self-administered). The questionnaire captures symptomatology, self-worth, self-efficacy, sense of belonging, and mindfulness.

Secondary

MeasureTime frame
Beck Depression Inventory (BDI-II): The BDI-II is a self-report instrument designed to assess the severity of depressive symptoms (T0, T1). Quality of Life - Globalitem (WHO-QOL-BREF): the global item of the self-assessment questionnaire measures quality of life (T0, T1). Rosenberg Self-Esteem Scale (RSES): the RSES is a self-report instrument that measures self-esteem (T0, T1). Global Assessment of Functioning (GAF): The GAF is a third-party assessment instrument and is used to assess a person's general level of functioning (T0, T1). Generalized Anxiety Disorder 7 (GAD-7): The GAD-7 is a self-report anxiety symptom instrument that serves as a screening tool to identify generalized (T0, T1). The Social Phobia Inventory (SPIN): the SPIN is a self-report instrument for self-assessment of social anxiety (T0, T1). The Comprehensive Inventory of Mindfulness Experiences (CHIME): the CHIME is a self-report instrument for self-assessment of different aspects of mindfulness (T0, T1). Dissociative Symptoms Questionnaire (FDS-20): The FDS-20 is a self-report instrument for assessing dissociative symptoms (T0, T1). The Borderline Symptom List 23 (BSL-23): The BSL-23 is a self-report scale designed to assess the level of intrapsychic distress in borderline patients (T0, T1). Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5): The PCL-5 captures self-report symptoms of PTSD (T0, T1). Level of Personality Functioning Scale-Brief Form (LPFS-BF): The LPFS-BF captures self-report personality functioning levels (T0). Personality inventory for DSM-5 brief form (PID-5-BF): The PID-5-BF captures maladaptive personality factors for diagnosing personality disorders in self-report (T0, T1). Frost Multidimensional Perfectionism Scale (FMPS): the FMPS captures self-reported perfectionism (T0, T1). General Self-Efficacy Expectancy Scale (SWE): The SWE captures patients' self-efficacy expectations (T0, T1).

Countries

Germany

Contacts

Public ContactAmir.Hosseyn Yassari

Universitätsklinikum Hamburg-Eppendorf

a.yassari@uke.de+4915222827161

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026