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Acute-REMOTION: REMOTION in Acute Psychiatric Care

Acute-REMOTION: a Randomized Controlled Pilot Trial to Investigate the Feasibility and Potential Effects of a Transdiagnostic Treatment to Reduce Symptom Severity and Improve Emotion Regulation in Acute Psychiatric Patient Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04990674
Acronym
Acute-REMOTION
Enrollment
60
Registered
2021-08-04
Start date
2021-08-09
Completion date
2023-07-18
Last updated
2023-07-25

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

Conditions

Mental Disorder

Brief summary

This study aims to examine REMOTION, an internet-based intervention aimed at reducing symptom severity and improving emotion regulation in an acute psychiatric inpatient care setting. REMOTION is currently being studied in an outpatient psychotherapy setting. This study aims to investigate feasibility and first effects of this intervention in inpatient psychiatric care.

Interventions

BEHAVIORALREMOTION

REMOTION is an internet-based program focusing on emotion regulation and aimed at reducing patient symptom severity and improving emotion regulation. It consists of six modules and the structure is based on the extended process model of emotion regulation by Gross (2015). The intervention is currently being studied in an outpatient psychotherapy setting (Bielinski et al., 2020).

BEHAVIORALTAU

Treatment as usual (TAU), refers to standard treatment in an acute inpatient care setting at the Universitäre Psychiatrische Dienste Bern. This treatment includes different standard inpatient psychiatric care components (integrative psychiatric care).

Sponsors

University of Bern
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* 18 or older * In acute inpatient care * With internet access * Informed consent given

Exclusion criteria

* Current participation in another specific emotion regulation intervention group * Current or history of psychotic disorders, bipolar disorder, mental retardation or organic mental disorders * Acute suicidality * Insufficient mastery of German language

Design outcomes

Primary

MeasureTime frameDescription
Change in general symptom severityAssessed at BaselineAssessed with the Brief Symptom Inventory 18 (BSI-18)

Secondary

MeasureTime frameDescription
Emotion regulation skillsAssessed at Baseline, then after 4 Weeks, after inpatient discharge (on average 24 days after inpatient intake), and after 8 WeeksAssessed with the Self-Report Measure for the Assessment of Emotion Regulation Skills (SEK-27)
Usability of REMOTIONAssessed after 4 weeks, after inpatient discharge (on average 24 days after inpatient intake), and after 8 WeeksAssessed with the System Usability Scale (SUS)
Satisfaction with REMOTIONAssessed after 4 Weeks, after inpatient discharge (on average 24 days after inpatient intake), and after 8 WeeksAssessed with the ZUF-8 (Fragebogen zur Messung der Patientenzufriedenheit) Questionnaire adapted for an internet-based program
Difficulties in emotion regulationAssessed at Baseline, then after 4 Weeks, after inpatient discharge (on average 24 days after inpatient intake), and after 8 WeeksAssessed with the Difficulties in Emotion Regulation Scale (DERS)
Qualitative interviews with healthcare workers4 months after study startRecorded interviews on the topic of attitudes towards / barriers and facilitators / advantages and disadvantages of internet-based interventions in inpatient care
Qualitative interviews with patients lost to follow upAfter a patient is lost to follow-up (after the 8 week timepoint when follow-up is assessed, has passed for the individual patient)Individuals lost to follow up can take part in a telephone interview on a voluntary basis, this examines reasons for loss to follow up
REMOTION usage parametersAssessed after 4 weeks, after inpatient discharge (on average 24 days after inpatient intake) and after 8 weeksAmount of modules completed and amount of exercises completed

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026