[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"psychosocial-stress\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:psychosocial-stress":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"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":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":5},"100628135","mygenesis-path-digital-program-for-donor-conceived-people-100628135",false,"NCT07457697","MyGENESIS-PATH: Digital Program for Donor-Conceived People","A Randomized Pilot and Feasibility Trial of a Digital Psychoeducational Intervention for Donor-Conceived Adults (MyGENESIS-PATH)","MyGENESIS-Path","Inclusion Criteria:\n\n* Donor-conceived people\n* Aged 18 or over\n* Able to read and understand English\n* Provide informed consent\n\nExclusion Criteria:\n\n* Previous participation in the MyGENESIS-PATH alpha-testing phase\n* Unable to provide informed consent\n* Unable to complete the online study procedures",true,"ALL","18 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","MyGENESIS-PATH is a self-guided digital psychoeducational intervention designed to support donor-conceived adults in navigating donor-conception-related information and uncertainty, DNA testing, identity, family relationships, disclosure, stigma, and expectations concerning donors and donor siblings.\n\nThis two-arm randomized pilot and feasibility trial will evaluate the feasibility and acceptability of delivering MyGENESIS-PATH and of conducting a future definitive randomized controlled trial. Sixty donor-conceived adults will be randomly allocated in a 1:1 ratio to immediate access to MyGENESIS-PATH or to a waitlist control condition.\n\nPrimary feasibility outcomes will assess recruitment, completion of the 4-week follow-up assessment, completeness of psychosocial outcome data, intervention uptake and completion, and completion of the immediate post-intervention feedback assessment. Intervention acceptability, usability, perceived usefulness, relevance, emotional manageability, and potential unwanted effects will be assessed among participants allocated to MyGENESIS-PATH.\n\nChanges in perceived stress, psychological well-being, coping, and donor-conception-related identity from baseline to 4 weeks after randomization will be examined as exploratory outcomes. The study is not powered to detect definitive intervention effects.",[28],"Psychosocial Stress",[30,31,32,33,34,35,36,37],"donor-conceived people","donor conception","Psychoeducational intervention","Digital intervention","Cognitive-behavioral training","Stress and coping","Psychological well-being","Randomized controlled trial","NOT_YET_RECRUITING","2026-07-15",{"date":41,"type":42},"2026-07-17","ACTUAL",{"date":44,"type":22},"2026-08-18",{"date":46,"type":22},"2026-11-30",{"name":48,"class":49},"Universidade do Porto","OTHER"]