[{"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-a-pilot-and-feasibility-trial-of-a-digital-intervention-for-donor-conceived-adults-100628135",false,"NCT07457697","MyGENESIS-PATH: A Pilot and Feasibility Trial of a Digital Intervention for Donor-Conceived Adults","A Randomized Pilot and Feasibility Trial of MyGENESIS-PATH, a Digital Psychoeducational Intervention for Donor-Conceived Adults","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* Not donor-conceived\n* Underaged ot minor\n* Unable to read and understand English\n* Unable to provide informed consent\n* Inability to complete online questionnaires \u002F lack of internet access",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 managing stress and navigating identity, information, family, DNA-testing, and donor- or sibling-contact-related experiences.\n\nThis 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 group. The primary objectives are to assess recruitment, retention, intervention uptake and completion, data completeness, acceptability, usability, and potential unwanted effects. Changes in perceived stress, psychological wellbeing, coping, and donor-conception-related identity will be explored to assess the suitability and variability of outcome measures and to inform the design of a future trial.",[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","2026-06-18",{"date":41,"type":42},"2026-06-24","ACTUAL",{"date":44,"type":22},"2026-07-01",{"date":46,"type":22},"2026-10-31",{"name":48,"class":49},"Universidade do Porto","OTHER"]