Skip to content

Single arm no-randomized open trial on feasibility and efficacy of internet-based acute treatment / recovery program for sexual assaulted victims with PTSD

Single arm no-randomized open trial on feasibility and efficacy of internet-based acute treatment / recovery program for sexual assaulted victims with PTSD - Research on internet-based program for sexual assaulted victims with PTSD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000026518
Enrollment
10
Registered
2017-03-15
Start date
2017-03-16
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

Posttraumatic Stress Disorder(PTSD)

Interventions

Internet-based program for sexual assaulted victims with PTSD

Sponsors

Musashino University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Those who had their first psychiatric examination following rape 2.Native Japanese speaker 3.Those who own a mobile device capable of using the program

Exclusion criteria

Exclusion criteria: 1.Those who cannot continue medical treatment due to psychiatric disorders (ex. schizophrenia, bipolar disorder, substance-related disorder, A cluster personality disorder, etc.) and psychiatric symptoms (severe psychotic symptoms, severe symptoms of depression, self-injury behavior, suicide attempt, etc.) 2. Those who have a physical disease in severe or unstable state

Design outcomes

Primary

MeasureTime frame
Impact of Event Scale Revised(IES-R)

Secondary

MeasureTime frame
1.Beck Depression Inventory -II (BDI -II) 2.Kessler10(K10) 3.Dissociative Experiences Scale(DES) 4.Posttraumatic Cognitions Inventory(JPTCI) 5.Satisfaction Survey 6.Dropout rate 7.Emergence of adverse event

Countries

Japan

Contacts

Public ContactRieko Konno

Musashino University Institution of Cognitive Behavioral Therapy and Research

cbtinst@musashino-u.ac.jp03-5530-7695

Outcome results

None listed

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