[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Tilburg University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":199},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,45,74,107,141,175],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100525879","psychoeducation-for-older-adults-with-autism-100525879",false,"NCT06127472","Psychoeducation for Older Adults With Autism","Support With Psychoeducation for Older Adults With Autism Study","OPAS","Inclusion Criteria:\n\n* minimum of 55 years old.\n* diagnosed with ASD or a probability diagnosis by a multidisciplinary team according to the Dutch multidisciplinary guideline, as confirmed by the DSM-5 interview for ASD (Spek, n.d.), or the Netherlands Interview for Diagnosis of ASD in adults (NIDA; Vuijk, 2023)\n\nExclusion Criteria:\n\n* comorbid mental disorder that needs acute treatment and severely interferes with a group treatment (for example psychosis),\n* a major neurocognitive disorder (for example dementia or acquired brain injury),\n* substance abuse disorder, that requires detoxification, and\u002For\n* an IQ below 70.",true,"ALL","55 Years",{"count":21,"type":22},120,"ESTIMATED","INTERVENTIONAL",[25],"NA","Until recently, autism in older adults went unrecognised. Although there has been more attention to autism in older adults in recent years, there is still a lot of unfamiliarity with the phenomenon and underdiagnosis in (mental) health care. Many care providers are reluctant to diagnose autism in later life, due to a lack of knowledge about autism in older adults and because there is still very little scientific knowledge available for this target group. Although several multidisciplinary guidelines for autism in adults prescribe that after the diagnosis psycho-education is the first step in treatment, psycho-education is still only offered in a few places in the Netherlands. Psycho-education is important to help older people gain knowledge about their autism, to help them understand and accept this diagnosis, in order to subsequently make the treatment of the problems, with which they turn to the mental health care, more appropriate and effective.\n\nThe aim of this study is to contribute to better recognition and diagnosis of autism among older adults. This research also aims to improve a psycho-education program for older adults and investigate its effects.\n\nThe scientific research question is whether training in ASD for health care professionals results in better recognition and detection of ASD in older adults, and whether participation in the psycho-education course for older adults, who have been diagnosed with autism, or have received a probability diagnosis ASD, contributes to improvement of mental health and quality of life.",[28],"Autism Spectrum Disorder",[30,31],"autism","older adults","RECRUITING","2026-05-13",{"date":35,"type":36},"2026-05-18","ACTUAL",{"date":38,"type":36},"2024-09-12",{"date":40,"type":22},"2027-03-31",{"name":42,"class":43},"Tilburg University","OTHER",11,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":18,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":23,"phases":55,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100619257","sensorimotor-psychotherapy-for-personality-disorders-100619257","NCT07342270","Sensorimotor Psychotherapy for Personality Disorders","SPiPS","Inclusion Criteria:\n\n* Aged 16 and older\n* Diagnosed with a personality disorder according to the DSM-classification\n* Has a history of early childhood trauma\n\nExclusion Criteria:\n\n* Does not master Dutch \u002F English sufficiently for filling out the questionnaire cannot fill participate in the research.\n* Presents factors or behaviour that disrupts participation in the group and undermines treatment will be excluded from this study.","16 Years",{"count":54,"type":22},131,[25],"SUMMARY\n\nRationale: Personality disorders are treated conform the Dutch GGZ-zorgstandaard mainly with verbal psychotherapies but experts by experience call out to make use of body-oriented approaches as well. In general, the rationale to study the effects of bodily centered therapy for personality disorders is built on the overlap between personality disorders and posttraumatic stress disorder (PTSD). In both classifications, childhood major events and\u002For traumatic life events play a role in the history of its origins (Karatzias et al., 2023).Traditional psychotherapies for personality disorders address the cognitive and emotional elements of trauma, but lack techniques that work directly with the physiological elements, although trauma profoundly affects the body and many symptoms of traumatized individuals with personality disorders are somatically based. However, studies into the effect of body centered interventions for personality disorders are scarce. This study aims to examine the effects of sensorimotor psychotherapy (SP), a body-oriented intervention, in patients with a personality disorder and PTSD-symptoms. This study studies the effect of sensorimotor psychotherapy (SP) which is a body-oriented intervention which focuses on the combination of a personality disorder and post-traumatic stress disorder.\n\nObjective: This multi-center randomized controlled study aims to research the effect of a 12-session sensorimotor psychotherapy (SP) group intervention, in comparison with treatment-as-usual, on emotion regulation in people with a personality disorder. In addition, the effects on body awareness, self-soothing, PTSD-symptoms and personality functioning are assessed. Patients' perception of the intervention will be assessed through qualitative techniques. The study will be carried out in five mental health institutions in the Netherlands.\n\nStudy design: This is a multi-center randomized controlled trial, in which the intervention group receives a 12-sessions SP-therapy, and the control group receives treatment-as-usual of the assigned institution. Measurements through standardized instruments take place at three moments: pre-intervention (T0), post-intervention (T1), and two months follow-up (T2). Qualitative interviews are conducted after completion of the SP-condition. In combination with the qualitative measurements, a Mixed Methods Design is used.\n\nStudy population: Patients older than 18 years, who have been diagnosed with a personality disorder and have experienced early childhood trauma.\n\nIntervention: patients assigned to the SP-condition receive the 12-session SP group protocol (Fisher \\& Ogden, 2016), this protocol introduces diverse successive skills, aiming for the patient to have more somatic resources to regulate arousal of the autonomous nervous system. Every session starts with psychoeducation on a trauma-related theme, followed by one or multiple skills which are practiced in dyads and are later discussed in the group. The subjects which are covered are: autonomous arousal, implicit memory, regulation techniques, survival sources, somatic and internal resources, boundaries, practicing with experiments and repetitions, focus on positive change.\n\nMain study parameter: The main parameter of this study is emotion regulation. Emotion regulation is examined with the Difficulties in Emotion Regulation Scale - Short Form (DERS-SF).\n\nSecondary parameters: Second parameters are body awareness, self-soothing, PTSD-symptoms, personality functioning. Body awareness is examined with the Multidimensional Assessment of Interoceptive Awareness (MAIA-2). The Soothing Receptivity Scale (SRS) is used to examine self-soothing abilities. The PTSD-checklist for DSM-5 (PCL-5) is used to assess the PTSD-symptoms. The Level of Personality Functioning Scale-Brief Form 2.0 (LPFS-BF 2.0) is used to map out personality functioning. The patients' perception of the intervention is explored through qualitative interviews. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients involved in this study are indicated for treatment for a personality disorder. Sensorimotor psychotherapy belongs the treatment options of some mental health institutions. Additionally, patients who are assigned to the control condition are offered the SP-condition after completing the control condition. In this way they can also benefit from the SP-condition.\n\nQuestionnaires are filled in at three moments during the treatment (T0, T1, T2), filling in the questionnaires will take 60 minutes on average, which is little more than routine outcome measurement takes in Dutch mental healthcare. The qualitative interviews after the SP-condition will take up 60 minutes on average.",[58,59],"Early Chilhood Trauma","Personality Disorder",[61,62,63,64],"Sensorimotor Psychotherapy","Personality disorders","Early childhood trauma","SP-protocol","NOT_YET_RECRUITING","2026-01-07",{"date":68,"type":36},"2026-01-15",{"date":70,"type":22},"2026-02-01",{"date":72,"type":22},"2028-12-31",{"name":42,"class":43},{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":81,"minAge":82,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":23,"phases":85,"briefSummary":86,"conditions":87,"keywords":91,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":106},"100503054","mother-infant-bonding-in-the-brain-a-mindfulness-based-intervention-100503054","NCT05830266","Mother-infant Bonding in the Brain: a Mindfulness-based Intervention","Mother-infant Bonding in the Brain: Promoting Maternal Mental Health and High-quality Mother-infant Interactions Via a Mindfulness-based Intervention","Inclusion Criteria:\n\n* Pregnant women (18+y).\n* First antenatal visit \\\u003C 12 weeks.\n* Score above cut off on the Edinburgh Postnatal Depression Scale (EPDS), the anxiety subscale of the Symptom Checklist (SCL-90) and\u002For the Parental Stress Questionnaire (PSQ) at 8-10 weeks postpartum.\n* Dutch-speaking or understanding Dutch.\n\nExclusion Criteria:\n\n* Gemelli pregnancy (or higher order pregnancy).\n* Known endocrine disorder before pregnancy (diabetes-I, Rheumatoid arthritis).\n* Severe psychiatric disease (schizophrenia, borderline or bipolar disorder).\n* HIV.\n* Drug or alcohol addiction problems.\n* Any other disease resulting in treatment with drugs that are potentially adverse for the fetus and need careful follow-up during pregnancy.\n* No access to the internet.","FEMALE","18 Years",{"count":84,"type":22},64,[25],"The study investigates the effectiveness of the mindfulness-based intervention \"Mindful with your Baby\" in women with babies between 5-9 months postpartum who experience heightened levels of postpartum depression, anxiety and\u002For parental stress. The intervention \"Mindful with your Baby\" is one of the very few interventions for maternal postnatal mental health issues that takes the bond between mother and infant into account. It is hypothesized that the \"Mindful with your Baby\" intervention will reduce levels of postpartum depression, anxiety and parental stress, and improve mother-infant behavioral interaction and increase neural synchrony between mother and infant brains.",[88,89,90],"Postpartum Depression","Postpartum Anxiety","Parental Stress",[92,93,94,95,96,97],"Postpartum depression","Postpartum anxiety","Parental stress","Mindfulness","Mindful with your baby","Mother-infant interaction","2025-09-15",{"date":100,"type":36},"2025-09-19",{"date":102,"type":36},"2023-07-01",{"date":104,"type":22},"2026-09",{"name":42,"class":43},1,{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":17,"sex":18,"minAge":115,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":118,"briefSummary":119,"conditions":120,"keywords":125,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":134,"lastUpdatePostDateStruct":135,"startDateStruct":137,"completionDateStruct":138,"leadSponsor":140,"locationsCount":4},"100596912","dino-study-daily-intervention-based-research-on-nurturing-opportunities-in-young-children-100596912","NCT07051642","Dino Study: Daily Intervention-based Research on Nurturing Opportunities in Young Children","The Dino Study: Rationale and Study Protocol for a Randomized Controlled Trial Evaluating the Incredible Years Dinosaur Program With Daily Assessments","Dino","Inclusion Criteria:\n\n* Children aged 4 to 8 years\n* At least one parent or primary caregiver willing and able to participate in the study and complete daily diary assessments\n* Sufficient Dutch language proficiency in child and parent to complete questionnaires and daily diary reports\n* Parental indication that the child shows elevated or (sub)clinical levels of conduct problems in daily life (e.g., frequent defiance, aggression, or rule- breaking behavior\n\nExclusion Criteria:\n\n* Intellectual disability in the child (IQ \\\u003C 70)\n* Child lives primarily in a different household during weekdays (e.g., institutional care, full-time co-parenting arrangement)\n* Parent\u002Fchild does not have sufficient Dutch language proficiency","4 Years","8 Years",{"count":21,"type":22},[25],"The goal of this clinical trial is to evaluate the effectiveness of the Incredible Years Dinosaur Program in children aged 4 to 8 years with conduct problems. The main questions it aims to answer are:\n\n* Does participation in the Dinosaur Child Program lead to greater improvements in children's emotional, social, and cognitive functioning, and reductions in externalizing behavior compared to a waitlist control group?\n* Does the intervention reduce emotional variability and daily behavior problems as captured through daily diary assessments?\n* Does the intervention improve daily parent-child dynamics, including reduced emotional escalation and more shared positive affect?\n\nResearchers will compare children in the intervention group to those in the waitlist control group to see if the program leads to better emotional regulation, fewer behavior problems, and improved parent-child interactions.\n\nParticipants will:\n\n* Be randomly assigned to either the intervention or waitlist control group (1:1) Receive 18 weekly small-group sessions (if in the intervention condition) using the Incredible Years Dinosaur Program\n* Complete daily diaries with their parent using the m-Path app during a 20-week period (baseline, intervention, follow-up)\n* Complete standardized pre- and post-intervention assessments via parent, teacher, and child reports",[121,122,123,124],"Behavior Problems in Children","Parent-Child Relations","Oppositional Behavior","Social Skills",[126,127,128,129,130,131,132,133],"Incredible Years Dinosaur Program","Conduct problems","Emotional sensitivity","Parent-child interaction","Daily diary","Experience Sampling Method","Randomized controlled trial","Behavioral intervention","2025-07-07",{"date":136,"type":36},"2025-07-10",{"date":98,"type":22},{"date":139,"type":22},"2026-04-30",{"name":42,"class":43},{"id":142,"slug":143,"hasResults":11,"nctId":144,"briefTitle":145,"officialTitle":146,"acronym":4,"eligibilityCriteria":147,"healthyVolunteers":17,"sex":18,"minAge":82,"maxAge":4,"enrollmentInfo":148,"targetDuration":4,"studyType":23,"phases":150,"briefSummary":151,"conditions":152,"keywords":156,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":174},"100575519","the-impact-of-playing-tetris-on-migrants-mental-health-100575519","NCT06773338","The Impact of Playing Tetris on Migrants' Mental Health","Does Playing Tetris Prevent the Development of Post-Traumatic Stress Disorder or Related Anxiety and Depressive Symptoms During and After Migration?","Inclusion Criteria:\n\n* Arabic-speaking immigrants of any gender who have applied for asylum in Greece or in the Netherlands, regardless of the outcome of their asylum application and their current residency status (rejected asylum seekers, recognized refugees, undocumented migrants).\n\nExclusion Criteria:\n\n* Minors (under the age of 18).",{"count":149,"type":22},300,[25],"This study examines if playing Tetris prevents the development of Post-traumatic stress disorder or related anxiety and depressive symptoms. The investigators recruit 300 participants in total in Greece and in the Netherlands. The participants are immigrants who have applied for asylum at any point in the past. The participants are asked to answer three questionnaires (on Post-traumatic stress disorder, related anxiety and depressive symptoms, and post-migration living difficulties) on a recurring basis - once every 4 weeks, 12 times in total. Half of the participants (treatment group) are randomly selected to play Tetris after completing the questionnaires. Participants in the treatment group are instructed to play Tetris for at least 15 minutes while trying to remember bad things that recently happened to them. Tetris is administered at three instances and participants in the treatment group are encouraged to play Tetris in case of experiencing any traumatic events or having any intrusive memories during the course of the study.",[153,154,155],"Post-traumatic Stress Disorder (PTSD)","Anxiety Symptoms","Depression Symptoms",[157,158,159,160,161,162,163,164,165],"Post-traumatic stress disorder","PTSD","Anxiety","Depression","Refugees","Asylum seekers","Migrants","Tetris","Longitudinal","2025-01-08",{"date":168,"type":36},"2025-01-14",{"date":170,"type":36},"2024-12-17",{"date":172,"type":22},"2025-12-07",{"name":42,"class":43},2,{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":179,"acronym":180,"eligibilityCriteria":181,"healthyVolunteers":11,"sex":18,"minAge":82,"maxAge":4,"enrollmentInfo":182,"targetDuration":184,"studyType":185,"phases":4,"briefSummary":186,"conditions":187,"keywords":189,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":106},"100256748","tilburg-health-outcomes-registry-of-emotional-stress-in-coronary-intervention-100256748","NCT02621216","Tilburg Health Outcomes Registry of Emotional Stress in Coronary Intervention","THORESCI","Inclusion Criteria:\n\n* PCI\n* Sufficient understanding of Dutch language\n\nExclusion Criteria:\n\n* life threatening comorbidity (e.g., metastasized cancer)\n* cognitive disorder",{"count":183,"type":22},3000,"10 Years","OBSERVATIONAL","Background of the study:\n\nPercutaneous coronary interventions (PCI) have become mainstay treatment for acute coronary artery disease and the number of patients receiving PCI is vastly growing. However, relatively little long-term follow-up studies of large real-world clinical samples exist that have looked at the real-world effects of PCI treatment and adherence to current guidelines.\n\nPsychological risk factors are important in determining prognosis after PCI, and undergoing PCI may increase the risk of low mood. To date, studies have examined single psychological risk factors, without taking into account their relatedness. Moreover, guidelines are advocating psychosocial screening in early cardiovascular disease, but the screening test as proposed in the prevention guideline has not yet been validated or tested. Although the detrimental effects of psychological risk factors on cardiovascular prognosis are known, the mechanisms through which they exert these effects are yet unclear. It is to be expected that not one but multiple biological (inflammation, endothelial dysfunction) and behavioural (coping styles, poor self-care, consultation behaviour) pathophysiological processes play a role, and that these processes interact with each other. In PCI patients the mechanisms linking psychological risk to poor prognosis are still to be investigated.\n\nObjective of the study:\n\n1. To examine the adherence to the prevention and PCI guidelines and the effects thereof on long term prognosis in PCI patients.\n2. To evaluate the effectiveness of the psychosocial screening instrument of the European Society of Cardiology Prevention guideline 2012.\n3. To examine effects of clustering psychological risk factors on several networks of potentially mediating mechanisms and long term outcomes in a large sample of PCI patients.",[188],"Coronary Heart Disease",[190],"percutaneous coronary intervention","2024-04-11",{"date":193,"type":36},"2024-04-15",{"date":195,"type":36},"2013-12-04",{"date":197,"type":22},"2037-12",{"name":42,"class":43},""]