[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"stress-related-disorders\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:stress-related-disorders":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,53],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100624299","step-by-step-back---a-feasibility-study-of-a-physical-activity-intervention-for-adults-with-stress-related-exhaustion-100624299",false,"NCT07407829","Step by Step Back - A Feasibility Study of a Physical Activity Intervention for Adults With Stress-related Exhaustion","Step by Step Back - A Feasibility Study of a CBT-Based Physical Activity Intervention for Stress-Related Exhaustion","Inclusion Criteria\n\n* Adult aged 20 to 64 years.\n* Experiencing stress-related exhaustion, assessed in regular clinical care (for example, symptoms consistent with exhaustion disorder or a closely related stress-related condition).\n* Symptoms are not in the acute phase (participant is able to engage in outpatient psychological treatment and gradual physical activity).\n* Elevated fatigue\u002Fexhaustion at screening, indicated by scores on screening questionnaires (Karolinska Exhaustion Disorder Scale and Multidimensional Fatigue Inventory).\n* Able to understand spoken and written Swedish.\n* Has access to a smartphone, tablet, or computer with an internet connection to complete study questionnaires and activity logging.\n* No medical condition that makes physical activity unsafe, based on clinical screening and participant self-report.\n\nExclusion Criteria\n\n* Currently receiving psychological treatment outside the recruiting clinic that is expected to interfere with participation in the program or study assessments.\n* Current or past diagnosis of a psychotic disorder.\n* Current or past diagnosis of bipolar disorder.\n* Severe mental health condition requiring another primary treatment approach at this time (for example, severe major depressive disorder, post-traumatic stress disorder, or an eating disorder).\n* Ongoing substance use disorder.\n* Medical condition or acute illness that makes physical activity inappropriate at this time (for example, recent blood clot, severe infection, or other serious condition).\n* Severe musculoskeletal condition that substantially limits ability to perform physical activity.\n* Started antidepressant medication within the past 4 weeks.\n\nAdditional notes (not eligibility criteria):\n\nParticipants may use psychotropic medication (for example, antidepressants, sleep medication, or anxiety medication) if the medication regimen is stable. Participants will be asked to report any medication changes during the study period. Mild to moderate comorbid anxiety or depression is allowed if stress-related exhaustion is the primary clinical problem.","ALL","20 Years","64 Years",{"count":20,"type":21},20,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical study is to learn whether a psychologist- or psychotherapist-guided physical activity program can be delivered and used as part of regular care for adults experiencing stress-related exhaustion. The program is designed to be integrated into regular psychological treatment as usual and supports participants in developing physical activity habits in a gradual, individualized, and sustainable way.\n\nThe main questions this study aims to answer are:\n\n* Can participants complete the program and attend the planned sessions?\n* Do participants and clinicians find the program acceptable, relevant, and useful?\n* Is the program safe, and do any negative experiences occur during the program?\n* What practical barriers and facilitators affect participation and delivery in routine care?\n* What descriptive patterns of change are seen in physical activity, symptoms, and everyday functioning from before to after the program?\n\nThe program is based on cognitive behavioral therapy (CBT) and acceptance and commitment therapy (ACT). It includes strategies to help participants set meaningful goals, take step-by-step actions toward those goals, and respond more flexibly to uncomfortable thoughts, emotions, and body sensations that may arise in relation to physical activity.\n\nAbout 12 to 20 participants will take part. The program is designed to be integrated into about 5 to 6 individual sessions delivered over a flexible time period, depending on each participant's pace and circumstances.\n\nParticipants will:\n\n* Take part in the physical activity program as part of their regular psychological treatment\n* Complete online questionnaires before and after the program\n* Log their physical activity during the program\n* Provide feedback after the program (and some participants will also take part in an interview)\n\nThe results will be used to assess whether the program is feasible and acceptable for participants and clinicians and to inform further refinement and future evaluation.",[27,28],"Exhaustion Disorder","Stress-Related Disorders",[30,31,32,33,34,35,36,37,38,39],"Stress-related exhaustion","Exhaustion disorder","Fatigue","Burnout","Physical activity intervention","Exercise therapy","Feasibility study","Cognitive behavioral therapy (CBT)","Acceptance and Commitment Therapy (ACT)","Psychological flexibility","RECRUITING","2026-02-05",{"date":43,"type":44},"2026-02-12","ACTUAL",{"date":46,"type":44},"2025-11-13",{"date":48,"type":21},"2026-10-01",{"name":50,"class":51},"The Swedish School of Sport and Health Sciences","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":16,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":4,"studyType":22,"phases":65,"briefSummary":66,"conditions":67,"keywords":71,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":52},"100578439","eeg-study-on-neurophysiological-and-psychological-effects-of-ericksonian-hypnotherapy-in-generalized-anxiety-disorder-100578439","NCT06811311","EEG Study on Neurophysiological and Psychological Effects of Ericksonian Hypnotherapy in Generalized Anxiety Disorder","Neurophysiological and Psychological Effects of Ericksonian Hypnotherapy on Generalized Anxiety Disorder: An EEG-Based Clinical Study","EEG-HypnoGAD","Inclusion Criteria:\n\n* Diagnosis of Generalized Anxiety Disorder (GAD) based on DSM-5 criteria\n* Aged 18-65 years\n* Capable of providing written informed consent\n* Fluent in Turkish (for hypnosis and assessments)\n* Not currently receiving psychotherapy or pharmacological treatment for anxiety\n\nExclusion Criteria:\n\n* Presence of comorbid psychiatric disorders (e.g., schizophrenia, bipolar disorder, major depression requiring immediate intervention)\n* History of neurological conditions (e.g., epilepsy, traumatic brain injury, stroke)\n* Current use of medications affecting EEG activity (e.g., benzodiazepines, SSRIs, antipsychotics)\n* Previous experience with hypnotherapy (to avoid expectancy bias)\n* Substance abuse or dependence within the last six months\n* Pregnancy or breastfeeding\n* Severe medical conditions that may interfere with participation","18 Years","65 Years",{"count":64,"type":21},60,[24],"This study examines the neurophysiological and psychological effects of Ericksonian hypnotherapy in individuals diagnosed with Generalized Anxiety Disorder (GAD). Using electroencephalography (EEG), the study aims to assess changes in brain activity and anxiety symptoms before and after treatment.\n\nA total of 60 participants will be recruited from both governmental and private psychiatric clinics in Istanbul. Participants will be randomly assigned to either the intervention group (receiving 12 Ericksonian hypnotherapy sessions over 12 weeks) or the control group (receiving no intervention).\n\nThe primary outcome measures include changes in EEG patterns, specifically alpha, theta, and frontal asymmetry indices, and changes in anxiety severity, measured by the Beck Anxiety Inventory (BAI), Generalized Anxiety Disorder-7 (GAD-7), and State-Trait Anxiety Inventory (STAI). Secondary measures include emotional regulation (DERS) and quality of life (WHOQOL-BREF).\n\nThis study aims to provide scientific evidence on the effectiveness of Ericksonian hypnotherapy as a complementary treatment for GAD and its impact on brain function and emotional well-being.",[68,69,70,28],"Generalized Anxiety Disorder (GAD)","Anxiety Disorders","Psychophysiological Disorders",[72,73,74,75,76],"Ericksonian Hypnotherapy","Hypnosis and Anxiety","EEG Neurophysiology","Anxiety Treatment","Cognitive-Emotional Regulation","2025-02-17",{"date":79,"type":44},"2025-02-20",{"date":81,"type":44},"2025-02-01",{"date":83,"type":21},"2025-09-01",{"name":85,"class":51},"Uskudar University"]