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Mindfulness, Empathy and the Oxytocinergic System in Persons With Schizophrenia

The Relationship Between Mindfulness and Empathy With the Oxytocinergic System in Persons With Schizophrenia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05491486
Acronym
OXYGEN
Enrollment
60
Registered
2022-08-08
Start date
2022-06-15
Completion date
2023-07-15
Last updated
2022-08-08

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

Conditions

Schizophrenia Spectrum and Other Psychotic Disorders

Brief summary

Recent studies indicated positive effects of mindfulness-based interventions (MBI) for schizophrenia (SCZ), but also on oxytocin (OXT) levels in healthy persons. It was also shown that response to MBI could be shaped by genetic factors. However, the interplay between mindfulness and empathy and genetic factors with the oxytocinergic system has not yet been examined in SCZ. The aim of the current explorative study is to (1) explore the effect of mindfulness-based group therapy (MBGT) on OXT levels as well as empathy in persons with SCZ; (2) investigate whether polygenic risk scores (PRS) for empathy can predict empathy levels in persons with SCZ; (3) investigate whether PRS for empathy and specific genetic configurations in the oxytocin receptors are associated with MBGT outcomes and OXT levels; 4) examine changes in positive- and negative symptoms, depression, anxiety, social functioning, and mindfulness at a within-group level and between both conditions. A parallel-group, proof-of-concept randomized controlled trial with 30 participants allocated to each trial arm (N = 60) will be conducted. Participants will be randomly assigned to MBGT alongside treatment as usual (MBGT+TAU) or treatment as usual (TAU). For a treatment period of four weeks, participants will receive weekly MBGT sessions. Four weeks after baseline assessments (T0), post-intervention assessments (T1) will take place. As a pilot study, effect sizes will be estimated for within- and between-group effects with corresponding confidence intervals. Outcomes of our proof-of-concept study can provide insight into potential biological mechanisms underlying mindfulness in SCZ, determine a valid biomarker associated with empathy and negative symptoms and pave the way for a personalized treatment approach for individuals with SCZ.

Interventions

Sponsors

Brain & Behavior Research Foundation
CollaboratorOTHER
Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

The condition will be revealed to the participants after all T0 assessments have been completed

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* be aged between 18 and 65 * meet diagnostic criteria for schizophrenia (ICD-10: F20.X) ascertained by a trained psychiatrist * sufficient German language proficiency to engage with the intervention * no recent (\<4 weeks) major change in psychopharmacologic medication * be able to give written informed consent

Exclusion criteria

* a score of 7 on any item of the positive scale of PANSS, suggesting severe psychotic symptoms * acute suicidality * current substance use other than nicotine * neurological disorders or brain damages

Design outcomes

Primary

MeasureTime frameDescription
Change in empathy levels EQBaseline and week 4Empathy Quotient (EQ) The EQ consists of 40 statements to which participants have to indicate the degree to which they agree or disagree. There are four response options: 'strongly agree', 'slightly agree', 'slightly disagree', 'strongly disagree'. 'Definitely agree' responses score two points and 'slightly agree' responses score one point on half the items, and 'definitely disagree' responses score two points and 'slightly disagree' responses score one point on the other half. The remainder of the response options score 0. Finally, Cronbach's alpha was 0.92, which is high.
Change in oxytocin levelsBaseline and week 4Venous blood samples will be taken to determine the basal oxytocin plasma to obtain an individual baseline and comparison level. Furthermore, saliva samples will be taken before and after each MBGT session to determine OXT levels.
Change in empathy levels IRIBaseline and week 4Interpersonal Reactivity Index (IRI) The IRI measures empathy on four subscales: perspective taking, fantasy, empathic concern and personal distress. Each subscale consists of 4 items rated on a 7-point Likert scale. The internal consistent is satisfactory with a Cronbach´s alpha of .78.

Secondary

MeasureTime frameDescription
Change in PANSS Positive, Negative, and General SymptomsBaseline and week 4The Positive and Negative Syndrome Scale (PANSS) is one of the most widely used rater instruments for the assessment of the presence and severity of psychotic symptoms. Each scale comprises seven statements which are rated by the interviewer using a seven-point Likert format (from 1= absent to 7= extreme). The PANSS is reported to have satisfactory internal consistency, good interrater reliability and construct validity.
Change in SNS Negative SymptomsBaseline and week 4This is a 20-item self-reported questionnaire with five subscales, namely alogia, avolition, anhedonia, social withdrawal and diminished emotional range. These subscales cluster on two factors, the apathy and emotional components. Participants can estimate the answer to each question on a scale from 0 (strongly disagree) to 3 (strongly agree). The scale was shown to have good internal consistency with Cronbach's alpha = .87.
Change in DASS Depression & AnxietyBaseline and week 4The 21-item Depression, Anxiety, and Stress Scale (DASS-21) is assessed on a four-point Likert-scale ranging from (0) did not apply to me at all over the last week to (3) applied to me very much last week. It shows internal consistencies of α \> 0.80 across the three subscales and has shown to be a useful measurement tool for patients with SSD.
Change in PANAS Positive and Negative AffectBaseline and week 4The PANAS contains 20 items, each consisting of an adjective describing an emotion. The participants have to select how applicable this adjective is to their current state from 1 (not at all) to 5 (extremely). Ten items are assigned to the positive (e.g. Excited) as well as the negative scale (e.g. Fearful). The reliability of the PANAS ranges from .86 to .93.
Change in BIRT Motivation (BMQ)Baseline and week 4The BIRT Motivation Questionnaire comprises 34 statements rated on a 4-point likert scale (always, often, sometimes, never). Internal consistencies of the BMQ-S and BMQ-R were high (Cronbach's alpha=.94 & .95 respectively).
Change in CFQ Psychological FlexibilityBaseline and week 4The instrument is self-reports, which showed high internal consistency in previous studies.
Change in SMQ MindfulnessBaseline and week 4The SMQ comprises 16 items that are rated on a seven-point Likert-scale ranging from (6) agree totally to (0) disagree totally. Consequently, the total score ranges from 0 to 96, with a higher score indicating higher mindfulness. The internal consistency of the German version of the SMQ was Cronbach's α = 0.89.
PSP Social FunctioningBaselineThe Personal and Social Performance Scale (PSP) is a rater-based questionnaire used to assess social functioning in patients with SSD. The PSP showed good test-retest reliability (ICC = 0.79) in patients with schizophrenia

Other

MeasureTime frameDescription
Polygenic Risk Scores (PRS)BaselineWe investigate whether polygenic risk scores (PRS) for empathy can predict empathy scores across groups at baseline in individuals with schizophrenia. For this purpose, the subject's genotypes will be examined. PRS have been shown to be associated with complex genetic traits such as empathy and mental disorders such as schizophrenia or autism spectrum disorders. Moreover, we will investigate whether empathy-PRSs and specific genetic configurations in the OXTR are associated with MBGT outcomes and OXT levels in blood samples on an exploratory level.

Countries

Germany

Contacts

Primary ContactKerem Böge, Dr. Dr.
kerem.boege@charite.de(+49)30 - 450 517636
Backup ContactNiklas Bergmann, M.Sc.
niklas.bergmann@charite.de(+49)30 - 450 517549

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026