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Exploratory study to determine predictive factors of effectiveness of interpersonal psychotherapy for mood disorder,anxiety disorder,post-traumatic stress disorder and eating disorder

Exploratory study to determine predictive factors of effectiveness of interpersonal psychotherapy for mood disorder,anxiety disorder,post-traumatic stress disorder and eating disorder - Exploratory study to determine predictive factors of IPT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022841
Enrollment
40
Registered
2016-07-01
Start date
2016-08-10
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

mood disorder,anxiety disorder,post-traumatic stress disorder,eating disorder

Interventions

interpersonal psychotherapy, 16weekly 60-minute sessions

Sponsors

Nagoya City University Psychiatry and Cognitive-Behavioral medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The Diagnosis is Depressive Disorders" or "Bipolar and Related Disorders" or "Anxiety Disoredrs" or "Post-traumatic stress disorder" or "Feeding and Eating disorders"for DSM-5. 2. The patients is on the waiting list. 3. The patients who can be signed informed concent were enrolled in the present study.

Exclusion criteria

Exclusion criteria: 1. The Diagnosis is "Schizophrenia Spectrum and Other Psychotic Disorders" or Obsessive-compulsive and Related Disorders" or "Cluster APersonality Disorders" or "Antisocial Personality Disorder" or "Neurodevelopmental Disorders" or "Neurocognitive disorders" 2. The patients who have active suicidal thought. 3. The patients who can't read and write questionnaire. 4. The patients who have any history of physical diseases or body condition that may prevent the study. 5. The patients who received or is going to receive other structured psychotherapy such as Cognitive-behavioral therapy. 6. Evidence of unable to participate half or more of the intervention phase. 7. The patients who their research doctor consider not suited.

Design outcomes

Primary

MeasureTime frame
mood disorder:Beck Depression Inventory-Second Edition(BDI-2) panic disorder:The Self-report Version of the Panic Disorder Severity Scale(PDSS-SR) social anxiety disorder:The Liebowitz Social Anxiety Scale Self Report(LSAS) PTSD:PTSD Diagnostic Scale(PDS) Eating disorder:Eating Disorder Inventory(EDI)

Secondary

MeasureTime frame
Social Adjustment Scale Self Report-SR(SAS-SR) State and Trait Anger Scale/Anger Expression Scale(STAXI) Interpersonal Sensitivity Measure(IPSM) Self Compassion Scale(SCS) IIP-64 Sheehan Disability Scale EQ-5D-5L Parental Bonding Instrument(PBI) Childhood Trauma Questionnaire(CTQ) Japanese Brief Grief Questionnaire Ten Item Personality Inventory(TIPI)

Countries

Japan

Contacts

Public ContactRisa Imai

Nagoya City University Psychiatry and Cognitive-Behavioral medicine

imai.r.nagoya@gmail.com052-851-5511

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026