[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"St.Gallen University of Applied Sciences\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":104},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,82],{"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":27,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":5},"100651740","nest-a-group-intervention-for-parents-with-complex-ptsd-100651740",false,"NCT07766265","NEST: A Group Intervention for Parents With Complex PTSD","NEST - Nurturing Emotional Safety in Trauma-Affected Parenting: A Pilot Feasibility and Acceptability Study of a Trauma-Informed Parenting Intervention for Parents With ICD-11 Complex Post-Traumatic Stress Disorder","Inclusion Criteria:\n\n* Diagnosis of CPTSD according to ICD-11, confirmed by the treating psychotherapist or psychiatrist\n* Caregiver of at least one child aged 0-18 years (including biological, adoptive, step-, or foster parents and other primary caregivers)\n* Currently receiving individual psychotherapeutic treatment (outpatient or inpatient setting)\n* Age 18 years or older\n* Sufficient German language proficiency to participate in group sessions and complete study questionnaires\n* Ability to provide written informed consent\n\nExclusion Criteria:\n\n* Current acute psychosis or severe psychiatric instability requiring immediate intensive treatment\n* Severe cognitive impairment or inability to participate adequately in group-based procedures\n* No current contact with the child\n* Insufficient German language proficiency","ALL","18 Years",{"count":19,"type":20},32,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this pilot clinical trial is to learn whether NEST, a new trauma-informed group therapy program, is feasible and acceptable for parents with Complex PTSD, a condition that can develop after prolonged or repeated traumatic experiences. Parenting can be especially challenging for people with this condition, and few treatment programs currently address this specific need. The main questions it aims to answer are:\n\n* Is the NEST group intervention feasible to deliver and acceptable to parents with Complex PTSD?\n* Do parents' trauma-related symptoms and their experience of the parenting role change from before to after the intervention?\n\nParticipants will:\n\n* Complete online questionnaires about trauma-related symptoms and parenting before the group therapy, after it ends, and again three months later\n* Take part in nine weekly 90-minute group therapy sessions, co-led by a member of the study team and a mental health professional from the treatment site\n* Some participants will additionally be invited to a short interview about their experience with the group therapy",[26],"Complex Post-Traumatic Stress Disorder",[26,28,29,30,31,32,33],"CPTSD","ICD-11","Trauma-Informed Intervention","Parents","Parenting Intervention","Group Therapy","NOT_YET_RECRUITING","2026-08-13",{"date":37,"type":38},"2026-08-14","ACTUAL",{"date":40,"type":20},"2026-08",{"date":42,"type":20},"2027-06",{"name":44,"class":45},"St.Gallen University of Applied Sciences","OTHER",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":64,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},"100592913","physical-activity-in-cancer-patients-in-an-oncology-day-clinic---implementing-a-person-centered-program-led-by-nurses-100592913","NCT06999616","Physical Activity in Cancer Patients in an Oncology Day Clinic - Implementing a Person-centered Program Led by Nurses","Promoting Physical Activity in Individuals With Cancer in an Oncology Day Clinic - Testing the Feasibility of the Implementation of a Physical Activity Concept Within an Interprofessional Team Led by Nurses OnkoMoveNurse - Proof of Concept","OnkoMoveNurse","Inclusion Criteria:\n\n1. diagnosis of cancer,\n2. at least three treatments at the oncology outpatient clinic in Münsterlingen during the study period,\n3. aged ≥18 years, and\n4. sufficient knowledge of German.\n\nExclusion Criteria:\n\n* pregnancy",{"count":55,"type":20},50,"OBSERVATIONAL","Background: Physical activity has demonstrated benefits in alleviating side effects and improving well-being in people with cancer. However, activity levels remain low during systemic treatment. Nurses are optimally positioned to lead interventions fostering an activity-friendly culture.\n\nObjective: This study aims to evaluate the feasibility and potential effects of the nurse-led, interprofessionally developed physical activity concept OncoMoveNurse in an outpatient oncology setting.\n\nMethods: Using a mixed-methods design over 15 months (10\u002F2024-12\u002F2025), the study includes implementation and evaluation phases. Quantitative data (n=50 patients, collected from 06\u002F2025-09\u002F2025) will assess primary (physical activity behavior) and secondary outcomes (self-efficacy, well-being, mood) via validated PROMs. Qualitative insights will be gathered through digital storytelling (n=2 patients, n=2 nurses) and one focus group (n=8 interprofessional team members). Inclusion criteria for patients include age ≥18, cancer diagnosis, at least three treatments in the day clinic, and sufficient German language skills.\n\nIntervention: OncoMoveNurse comprises five adaptable components: modular activity structure, safety framework, communication strategy, a team approach, and person-centered orientation. Supporting materials (e.g., posters, videos, exercise tools) and tailored implementation strategies were co-developed in alignment with core values.\n\nAnalysis: Quantitative data will be analyzed using SPSS (paired t-tests, p\\\u003C.05); qualitative data via content analysis in MAXQDA. A mixed-methods synthesis will integrate findings.\n\nEthics \\& Data Protection: Patient data collection will commence following ethics approval. All data are anonymized, stored securely, and handled in accordance with Swiss data protection laws.\n\nConclusion: This study will provide insights into the feasibility of nurse-led physical activity promotion in outpatient oncology and inform future outcome evaluations.",[59,60,61,62,63],"Neoplasms","Motor Activity","Chemotherapy","Antitumor Drugs","Activity Level",[65,66,67,68,69,70,71],"activity promotions","proof-of-concept","implementation","activity concept","excercise","cancer patient","physical activity","RECRUITING","2025-12-03",{"date":75,"type":38},"2025-12-10",{"date":77,"type":38},"2025-08-01",{"date":79,"type":20},"2026-08-31",{"name":44,"class":45},1,{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":88,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":90,"targetDuration":4,"studyType":21,"phases":92,"briefSummary":93,"conditions":94,"keywords":4,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":81},"100551780","evaluation-of-the-efficacy-of-compression-with-tight-surgical-gloves-in-patients-with-taxane-based-therapy-100551780","NCT06464536","Evaluation of the Efficacy of Compression With Tight Surgical Gloves in Patients With Taxane-based Therapy","Tight Surgical Gloves to Prevent Chemotherapy-induced Peripheral Neuropathy: A Randomized Controlled Trial to Evaluate the Efficacy of Compression Therapy in Patients With Taxane-based Chemotherapy for Breast and Urogenital Cancer","ComPrendo","Inclusion Criteria:\n\n* Mamma or Urogenital carcinoma\n* first treatment with Taxanes (nab-Paclitaxel, Paclitaxel, Docetaxel)\n* signed informed consent\n* sufficient proficiency in German or English\n\nExclusion Criteria:\n\n* other therapy that could have caused peripheral neuropathy within the last 24 months (Taxane, Platin, Vincaalkaloids, etc.)\n* History of neuropathy such as Raynaud's phenomenon, fibromyalgia and diabetic polyneuropathy\n* Use of polyneuropathy medications including duloxetine; gabapentin\u002Fpregabalin; topical amitriptyline, ketamine, baclofen; oral cannabinoids; tricyclic antidepressants; and ganglioside monosialic acid\n* such impaired cognition that prevents participation in the study according to the assessment of the caregivers",{"count":91,"type":20},114,[23],"In this study, the effect of compression therapy of the hands with tight surgical gloves to reduce peripheral neuropathy in adult patients during the application of taxanes will be evaluated.",[95],"Taxane-induced Peripheral Neuropathy","2025-05-13",{"date":98,"type":38},"2025-05-16",{"date":100,"type":38},"2025-02-03",{"date":102,"type":20},"2026-03",{"name":44,"class":45},""]