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Dynamic modelling of resilience: Interventional study.

Dynamic modelling of resilience: Interventional study. - DynaMINT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON52021
Enrollment
55
Registered
2022-06-08
Start date
2022-06-28
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

stress-gerelateerde klachten Stress-related mental health problems

Interventions

Participants will be randomly allocated to receive either an EMI that boosts positive reappraisal (ReApp) or an EMI that boosts reward sensitivity (Imager).

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Participants are healthy students (18-27 years old) who have experienced at least three life events which were each evaluated as burdening. Participants have a total GHQ (i.e. general health questionnaire) score >= 20. Volunteers are proficient in the Dutch language.

Exclusion criteria

Exclusion criteria: The participant currently meets criteria of a relevant psychiatric disorder except for a mild depressive episode (ICD F32.1), tobacco dependence (ICD F12) and substance abuse as established using the Mini-International Neuropsychiatric interview. The participant has met criteria for a relevant psychiatric disorder except for a mild depressive episode (ICD F32.1), tobacco dependence (ICD F12), and a substance abuse in the past 9 months. The participant has ever been diagnosed with a severe mental or organic disorder that affects neurodevelopment due to its pathological mechanism or treatment. The subject*s body mass index is lower than 18 or higher than 27. The participant is not eligible for functional magnetic resonance imaging. The participant reports the use of alcohol 24 hours before the second test baseline test battery. The participant took any psychoactive substances 4 weeks prior to the first or second baseline test battery. The participant is not eligible to wear the Chill+ or eligible for functional MRI. The participant is not free of COVID-19 related symptoms.The participant is currently in psychiatric treatment. The participant receives hormonal treatment other than oral contraceptives and/or takes steroids. The participant has participated in the DynaMOBS study, and/or any study including a fear conditioning and/or stress induction paradigm, and/or any study using an EMI similar to ReApp or Imager. The participant has a full beard.

Design outcomes

Primary

MeasureTime frame
The main study parameter is dynamic stress resilience as measured with a residuals-based stressors reactivity score.

Secondary

MeasureTime frame
Changes in resilience in relation to the given EMI are associated with biological parameters, psychological questionnaires, neuroimaging, and ecological momentary & physiological assessments.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)