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KopOpOuders for PTSD: Randomized controlled trial of a blended care preventive parenting intervention for parents with PTSD.

KopOpOuders for PTSD: Randomized controlled trial of a blended care preventive parenting intervention for parents with PTSD. - KopOpOuders-PTSD: Effectiveness of a course for parents with PTSD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51894
Enrollment
142
Registered
2021-12-16
Start date
2022-06-02
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

PTSD trauma traumatic stress

Interventions

The intervention group receives KOO-PTSD, consisting of 5 online modules and 3 face-to-face sessions, in addition to treatment as usual. The control group does not receive intervention apart from tr

Sponsors

Arkin (Amsterdam)
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: • Has current DSM-5 diagnosis of PTSD; • Is receiving PTSD treatment of at least three sessions at one of the following Arkin departments: Sinai Centrum, Jellinek, Punt P, NPI, or Arkin BasisGGZ; • Has parenting responsibilities for at least one child aged 4-17 (biological or legal relationship not required);

Exclusion criteria

Exclusion criteria: • Has urgent care needs or (imminent) crisis (e.g. current psychosis, substance detoxification, active suicidality); • Is not in contact with children (e.g. due to out of home placement) • Is receiving another form of parenting intervention during the participation period; • Severe psychological problems are present in children (diagnosis of oppositional-defiant disorder, conduct disorder, psychotic spectrum disorder or personality disorder); • Inability to participate in the intervention and/or assessments (e.g., because of mental disability (IQ

Design outcomes

Primary

MeasureTime frame
Primary study parameters are parenting behavior at the macro- and micro-level.

Secondary

MeasureTime frame
Secundary study parameters are sense of parenting competence, social support, parenting stress, psychosocial wellbeing of the child, and PTSD symptoms of the child. The following variables are also measured: parental PTSD symptoms, trauma type/timing, psychosocial functioning, demographic information of the parent and child, number of completed modules/sessions, number of interactions with PTSD-specific online intervention content, satisfaction with the intervention, sleep quality, situational context, and distress level.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)