No registrations found.
ID
Source
Brief title
Health condition
Depressive disorder
In Dutch: depressieve stoornis
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameter is the difference in feelings of self-stigma, as measured by the Internalized Stigma of Mental Illness scale, before and after psychoeducation, after 1 week and after 10 weeks.
Secondary outcome
Secondary parameters include perceived social support, loneliness and depressive symptoms for the patient and burden of care and quality of life for relatives.
Background summary
Rationale: Depression is a prevalent mental disorder, causing tremendous suffering for those affected and their relatives. Patients with depression often deal with stigma. We developed a virtual reality (VR) environment to experience a depression from the perspective of a patient and her relative (VR depression experience). We hypothesize that when patients and their relative experience the VR in a psychoeducation session, this will lead to less selfstigma, an increase in perceived social support, less loneliness and consequently less depressive symptoms for patients.
Objective: The main objective is to test whether our newly implemented VR psychoeducation protocol is more successful in reducing feelings of self-stigma than the standard psychoeducation protocol for depression. The secondary objectives are to investigate the effect of the VR depression experience on perceived social support, loneliness and depressive symptoms for the patient and burden of care and quality of life for the family.
Study design: We will conduct a randomized controlled trial at mental health care institution GGZ Delfland. Patients will be randomly assigned to one of the two conditions; the VR psychoeducation protocol or the standard psychoeducation protocol. In this study, we aim to show first evidence of the added benefit of the VR experience. The patients will fill in questionnaires before and after the psychoeducation session, after 1 week and after 10 weeks during their further psychological treatment.
Study population: In this study we assess 40 patients, with a relative of their choice, who will receive the VR psychoeducation protocol and 40 patients, also with a relative of their choice, who will receive the standard psychoeducation protocol. Patients will be male and female adults, aged 18 to 65 and diagnosed with a depression who are referred for psychotherapy for depressive disorder.
Study objective
We hypothesize that when patients and their relative experience the VR in a psychoeducation session, this will lead to less self-stigma, an increase in perceived social support, less loneliness and consequently less depressive symptoms for patients. We also hypothese that the VR experience will lead to a decrease in perceived burden of care, and an increase in quality of life of the relative.
Study design
Participants will fill in questionnaires before and after the psychoeducation session, after 1 week and after 10 weeks during their further psychological treatment.
Intervention
In both conditions, patients and their relative receive psychoeducation. This is manualized and consists of an explanation of the symptoms, possible causes, diagnosis and treatment of depression according to the Dutch CBT protocol book ‘Protocollaire behandelingen voor volwassenen’, section depressive disorder.
In addition to the above, in the VR psychoeducation condition, patients and relatives also watch the VR depression experience video. This consists of two 360º videos which summarize multiple fragments of a day in the life of a female depressive patient (1) from her perspective and (2) from the perspective of her male partner. The VR-experience includes getting up in the morning, having breakfast, interaction with the partner, sitting around in the afternoon not being able to undertake an activity and taking medication through the eyes of the patient whilst hearing her inner thoughts. The relative watches the video from the patient’s perspective, this takes 6 minutes. The study participant has the possibility to watch along on a screen. The study participant watches the VRexperience from the perspective of the partner, this experience takes 4 minutes in total. This experience includes mainly the same scenes; getting up in the morning, having breakfast, the evening after the partner returns from his job. This time, the study participant watches the scenes whilst hearing the inner thoughts of the partner, and the relative of the study participant has the possibility to watch along on a screen. After both the study participant and the relative have undergone the VR depression experience, the study participant and the relative will answer some questions related to the VR experience and the therapist will stimulate a mutual discussion about the content of the experience.
Inclusion criteria
• A principal diagnosis of depression (all severities), either a first or recurrent episode, as determined by a BIG registered psychologist (clinical or GZ) or psychiatrist
• Age between 18-65
• Willing to involve a relative (partner, friend, family member)
• Scheduled to start psychotherapy individually or in a group
• Written informed consent by both the patient and the relative to participate in the study
Exclusion criteria
• Intellectual disability in the history
• Severe comorbid psychiatric disorders including schizophrenia-like disorders, bipolar disorder or addictive disorders
• Abnormal hearing or uncorrected vision
Design
Recruitment
IPD sharing statement
Plan description
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL9070 |
CCMO | NL74955.018.20 |
OMON | NL-OMON55901 |