[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"interoception\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:interoception":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,78,105],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100053335","interoceptive-intervention-for-congenital-heart-disease-100053335",false,"NCT07697755","Interoceptive Intervention for Congenital Heart Disease","A Randomised Controlled Feasibility Trial Exploring an Interoceptive-Based Intervention in Patients With Congenital Heart Disease","Inclusion Criteria:\n\n* Participants must be aged 18 years or older\n* Under the care of the Scottish Adult Congenital Cardiac Service (SACCS) at the Golden Jubilee University National Hospital (GJUNH)\n* Be able to understand and communicate in English\n* Provide informed consent\n* Access and use a device compatible with Microsoft Teams\n* Be able to commit to the duration of the group programme\n\nExclusion Criteria:\n\n* Individuals with current suicidal ideation\n* Individuals with comorbid alcohol or substance use disorders\n* Individuals with a diagnosed learning disability\n* Individuals with a severe and enduring mental health condition (e.g., personality disorder or psychosis)\n* Individuals with hearing, visual and cognitive difficulties preventing safe online group participation\n* Individuals who are currently on a surgical or transplant waiting list\n* Individuals who are receiving intensive psychological treatment (e.g., trauma processing or crisis support)","ALL","18 Years",{"count":19,"type":20},32,"ESTIMATED","INTERVENTIONAL",[23],"NA","Adults living with congenital heart disease (CHD) commonly experience physical symptoms alongside emotional and social challenges, which can affect wellbeing and health-related quality of life. Access to psychological services varies, and evidence to guide the development and delivery of psychological interventions for this population is still emerging.\n\nInteroceptive-based approaches focus on increasing awareness of and responding adaptively to internal bodily sensations, such as breathing, heart rate and fatigue. These approaches have shown benefits in other long-term health conditions but have not yet been studied in adults with CHD. This study will evaluate the feasibility, acceptability, and preliminary effects of a newly adapted online, skills-based group programme for adults with CHD.\n\nThirty-two participants will be recruited through the Scottish Adult Congenital Cardiac Service and randomly allocated to one of two cohorts: Cohort 1 (Immediate Intervention) and Cohort 2 (Delayed\u002FWaitlist Intervention). The group programme will consist of eight online sessions delivered by a Principal Clinical Psychologist and a Trainee Clinical Psychologist. Weekly sessions will explore the relationship between interoception and key areas relevant to living with CHD, including emotions, behaviours, and physical symptoms. Group discussions and exercises will focus on increasing awareness and understanding of internal bodily sensations, developing strategies for responding to interoceptive cues and using bodily information to guide behaviours and everyday activities.\n\nParticipants will complete online questionnaires before and after the intervention assessing interoception, anxiety, depression and health-related quality of life. Participants will also provide feedback regarding the acceptability and perceived usefulness of the programme. Participation is voluntary, and participants may withdraw at any time without affecting their clinical care. Appropriate emotional support will be available should participants experience distress related to the group materials or discussions.\n\nFindings from this feasibility randomised controlled trial will inform further refinement of the group programme, assess the acceptability and feasibility of study procedures, provide estimates of recruitment, retention and outcome variability, and support the design and sample size calculation of a future definitive trial. The findings may also contribute to the enhancement of psychological support for adults with CHD and be disseminated through scientific publications and conference presentations.",[26,27],"Interoception","Congenital Heart Disease",[29,26,30,31,32,33],"Adult Congenital Heart Disease","Psychological Intervention","Group Intervention","Pilot Study","Feasibility Randomised Controlled Trial","NOT_YET_RECRUITING","2026-07-08",{"date":37,"type":38},"2026-07-13","ACTUAL",{"date":40,"type":20},"2026-07",{"date":42,"type":20},"2026-12",{"name":44,"class":45},"University of Glasgow","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":58,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":46},"100541676","interoceptive-mechanisms-of-body-image-disturbance-in-anorexia-nervosa-100541676","NCT06332963","Interoceptive Mechanisms of Body Image Disturbance in Anorexia Nervosa","Inclusion Criteria:\n\n1. Primary diagnosis of anorexia nervosa\n2. Photographic Figure Rating Scale (PFRS) body dissatisfaction score greater than or equal to 1\n3. Eating Disorder Examination Questionnaire (EDE-Q6) Shape Concern Subscale score greater than or equal to 3\n4. Weight restored to body mass index (BMI) greater than or equal to 17.5\n5. No current evidence of orthostatic hypotension or if there is no evidence of additional fall risk as determined by their provider\n6. Clinical status transition from acute to residential status\n7. No new psychiatric medications in the week prior to randomization\n8. Female sex assigned at birth\n9. Ages 13 to 50 years\n10. Independently ambulatory\n11. Ability to lay flat comfortably\n12. English proficiency\n13. Willingness and ability to participate in study procedures\n14. Provision of informed consent (parent consent and minor assent if less than 18 years of age).\n\nExclusion Criteria:\n\n1. Active suicidal ideation with plan and intent\n2. Active cutting or skin lacerating behaviors\n3. Pregnancy as defined by urine screening\n4. Acute intoxication as indicated by urine drug screen or breathalyzer\n5. Orthostatic hypotension as determined by medical provider, evidenced in chart (defined as a drop of ≥ 20 mmHg in systolic blood pressure (BP) or a drop of ≥ 10 mm Hg in diastolic blood pressure (BP) when measured shortly after transitioning from lying down to standing). If evidence of orthostasis is present in chart consultation with provider to determine if status creates additional fall risk. If participant is determined to be at increased fall risk (e.g., dizziness upon standing) they will be excluded.\n6. Seizure reported within the previous 12 months\n7. Co-morbid diagnoses of Diagnostic and Statistical Manual of Mental Disorders, 5th ed. (DSM-5) bipolar disorder, schizophrenia, or other psychosis spectrum disorder\n8. Systolic blood pressure \\> 160 mmHg\n9. Diastolic blood pressure \\>100 mmHg\n10. Resting heart rate \\<50 beats per minute.","FEMALE","13 Years","50 Years",{"count":57,"type":20},102,[23],"The proposed study utilizes a randomized experimental therapeutics design to test a mechanistic framework linking interoceptive processing and disturbed body image, with the purpose of informing the development of future therapies for body image dissatisfaction in anorexia nervosa (AN). A sample of 102 participants will be recruited from the Laureate Eating Disorder Program (LEDP). After being randomized, participants will all receive a one-hour session of acceptance- and mindfulness-based training with a therapist (the introduction session). They will then receive either the interoceptively focused treatment (IFT) or exteroceptively focused treatment (EFT) condition based on randomization. In the IFT condition participants will engage in floatation-REST (Reduced Environmental Stimulation Therapy) while practicing acceptance and mindfulness-based principles. The EFT condition is an exteroceptive intervention in which participants will be asked to view pre-recorded videos of acceptance and mindfulness-based skills to aid in the practice of these skills. Each condition will consist of one introduction session and three experimental sessions. All participants will then return for follow-up measures. Assessed outcomes will include acute changes in body image disturbance (BID) and interoception. Further, longitudinal intervention effects on self-reported eating disorder symptoms, body image dissatisfaction, and interoception; behavioral measures of interoception and body image dissatisfaction; and resting state and interoceptive functioning during functional magnetic resonance imaging (fMRI) will be explored.",[61,62,26],"Anorexia Nervosa","Body Image Disturbance",[61,62,64,26,65,66,67],"Perceptual Body Image","Acceptance Based Intervention","Mindfulness Based Intervention","Randomized Clinical Trial","RECRUITING","2025-09-25",{"date":71,"type":38},"2025-09-26",{"date":73,"type":38},"2024-04-19",{"date":75,"type":20},"2028-12",{"name":77,"class":45},"Laureate Institute for Brain Research, Inc.",{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":84,"eligibilityCriteria":85,"healthyVolunteers":86,"sex":53,"minAge":17,"maxAge":87,"enrollmentInfo":88,"targetDuration":4,"studyType":21,"phases":90,"briefSummary":91,"conditions":92,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":46},"100589919","nature-for-body-image-100589919","NCT06960668","Nature for Body Image","Look at the Bright (Nature) Side: Improving Body Image and Associated Protective Factors and Reducing Body Image Threats With the Nature for Body Image (NBI) Project","NBI","Inclusion Criteria:\n\n* Females\n* Age 18-35 years old\n\nExclusion Criteria:\n\n* Full-blown body image disorder",true,"35 Years",{"count":89,"type":20},60,[23],"Nature exposure has been found to be particularly beneficial for body image, as recent studies have identified a positive association between time spent in nature and positive body image. Positive body image, defined as the ability to accept and respect one's body, has been linked to greater life satisfaction and engagement in healthy behaviors. Conversely, negative body image is recognized as a public health concern due to its detrimental effects on both physical and mental health. It has been associated with symptoms of Body Image Disorders (BIDs), including Eating Disorders (EDs) and Body Dysmorphic Disorder (BDD).\n\nThe Nature for Body Image (NBI) project aimed to examine the impact of a structured nature exposure intervention on improving body image among young women aged 18-35 years.",[93,94,95,26],"Body Image","Eating Behaviors","Self-Compassion","2025-05-15",{"date":98,"type":38},"2025-05-16",{"date":100,"type":38},"2025-05-01",{"date":102,"type":20},"2026-02-28",{"name":104,"class":45},"University of Padova",{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":21,"phases":113,"briefSummary":114,"conditions":115,"keywords":117,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":46},"100550169","interoceptive-intervention-for-pulmonary-hypertension-100550169","NCT06443580","Interoceptive Intervention for Pulmonary Hypertension","The Relationship Between Interoception and Psychological Outcomes: A Mind-Body Intervention in Patients With Pulmonary Hypertension","Inclusion Criteria:\n\n* Participants will be patients under the care of the Scottish Pulmonary Vascular Unit (SPVU) at the Golden Jubilee University National Hospital (GJUNH).\n* Diagnosed with any type of PH.\n* Adults over 18 years.\n* Fluent in English.\n* Able to commit to the duration of the research (expected to be three months from initial recruitment to the end of treatment).\n\nExclusion Criteria:\n\n* Individuals with current thoughts of self-harm or suicide.\n* Presenting with comorbid alcohol or substance misuse.\n* Currently engaging in any additional psychological interventions at the time of the study.",{"count":19,"type":20},[23],"Background Pulmonary hypertension is a rare and incurable condition characterised by fatigue and breathlessness. The effects of pulmonary hypertension has a significant impact on an individual's emotional wellbeing and there are currently no established psychological interventions to improve this. Interoception is defined as the ability to perceive the internal state of the body and emerging research suggests that interventions to improve interoception can improve well-being.\n\nAims The project aims to develop an interoceptive based intervention for those with pulmonary hypertension and examine the feasibility and acceptability of this. Additional aims are to explore the preliminary results of the intervention.\n\nMethods A randomised control feasibility trial will be used. Thirty-two participants will be included. Participants will be patients within the Scottish Pulmonary Vascular Unit diagnosed with pulmonary hypertension and randomly assigned to either the intervention or control (waitlist) group. The intervention will be an eight-session online group and participants will complete measures for interoception, anxiety, depression, health related quality of life, as well as a feasibility and acceptability questionnaire. Quantitative analysis will include descriptive statistics and T-tests (including non-parametric versions) to analyse the feasibility and gain a preliminary understanding of the intervention.\n\nPractical Applications It is hoped that the findings will identify a sample size for a larger trial whilst also informing future clinical practice. This project will be written up for a suitable journal and will be presented at an appropriate conference.",[26,116],"Pulmonary Hypertension",[118,119],"interoception","pulmonary hypertension","2025-03-10",{"date":122,"type":38},"2025-03-11",{"date":124,"type":38},"2024-06-17",{"date":126,"type":20},"2025-10-18",{"name":128,"class":129},"Golden Jubilee National Hospital","OTHER_GOV"]