[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Qatar University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":105},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,72],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":5},"100590093","an-online-physical-activity-coaching-intervention-for-people-with-pd-in-qatar-100590093",false,"NCT06962930","An Online Physical Activity Coaching Intervention for People With PD in Qatar","A Pilot RCT of a Remote Physical Activity Coaching Intervention to Promote Engagement in Physical Activity for People With Parkinson's Disease in Qatar","EQP","Inclusion Criteria:\n\n1. Age above 18 years.\n2. Successful completion of Physical Activity Readiness Questionnaire (PAR-Q), or medical clearance from a neurologist.\n3. Ambulatory for indoor and outdoor mobility with or without an assistive device but without physical assistance.\n4. A neurologist-confirmed diagnosis of PD.\n5. Ability to follow study-related commands.\n\nExclusion Criteria:\n\n1. Musculoskeletal injury or a medical condition that would prevent safe participation in an exercise program including failure to pass the PAR-Q test.\n2. The presence of any other neurological conditions.\n3. Acute illness or injury that prevents participation in the intervention.","ALL","18 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","Regular exercise can improve function and quality of life as well as have other positive behavioral and health-related benefits in people Parkinson's disease (PD). Despite the benefits, insufficient exercise is common among PD individuals, often due to common barriers, emphasizing the importance of empowering individuals with adequate knowledge and self-management skills.\n\nThis project aims to develop \"Engage-Qatar PD,\" an online physical activity self-management program for people with PD in Qatar. Engage-Qatar PD will be grounded in a previously developed coaching intervention used in people with Huntington's disease (Engage HD) and people with PD. The main focus of this project will be the development work to adapt this intervention for online delivery for people with PD and within the Qatari context.\n\nThis development stage will entail participatory design, in which users will be actively involved as co-designers to ensure fully the required cultural adaptations. Following this development phase, a pilot randomized controlled trial will be conducted to assess the feasibility, acceptability, and potential benefits of the developed intervention.\n\nThe innovative approach proposed for this project would have wide-reaching impact, advancing the development of new therapeutic options. It will deliver a realistic, culturally adapted therapeutic option for people with PD in Qatar that has the potential to be implemented in a variety of healthcare settings and other countries in the region. Importantly, future work could replicate this program in a larger cohort of individuals with other neurodegenerative diseases and extend this work to other countries in the region.",[27],"Parkinson Disease",[29],"PD: Parkinson's Disease PA: Physical Activity NDD: Neuro Degenerative Disease QRI: Qatar Rehabilitation Institute","RECRUITING","2025-09-23",{"date":33,"type":34},"2025-09-29","ACTUAL",{"date":36,"type":34},"2025-09-10",{"date":38,"type":21},"2026-09-10",{"name":40,"class":41},"Qatar University","OTHER",{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":17,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":54,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":4},"100585624","treatment-outcomes-of-pulpotomy-versus-pulpectomy-in-vital-primary-molars-diagnosed-with-irreversible-pulpitis-100585624","NCT06904781","Treatment Outcomes of Pulpotomy Versus Pulpectomy in Vital Primary Molars Diagnosed With Irreversible Pulpitis","Treatment Outcomes of Pulpotomy Versus Pulpectomy in Vital Primary Molars Diagnosed With Symptomatic Irreversible Pulpitis: A Non-inferiority Randomised Controlled Trial","Inclusion Criteria:\n\n1. Healthy (ASA I and II) co-operative children (Frankl Scale + and ++) between the ages of four and nine years.\n2. Participants have symptoms typical of irreversible pulpitis in one of the primary molars.\n3. The pulp of the affected primary molar is vital.\n4. Radicular pulp health is confirmed by attainment of radicular pulp haemostasis within 6 minutes of coronal pulp amputation.\n5. The affected primary molars can be restored with full coverage stainless steel crowns.\n6. Any physiologic root resorption, if present, is less than ⅓ the root length.\n\nExclusion Criteria:\n\n1. Clinical examination of affected primary molar reveals signs of pulpal infection (e.g. pathologic tooth mobility, parulis\u002Ffistula, or soft tissue swelling).\n2. Pre-operative periapical radiograph suggests presence of periapical radiolucency or pathologic root resorption.\n3. Visual examination of pulp tissue after deroofing reveals signs of necrosis (e.g. avascular\u002Fminimally bleeding pulp tissue or yellowish necrotic areas\u002Fpurulent exudate).\n4. Signs of extensive radicular pulp inflammation i.e., root pulp bleeding continues even after 6-min.\n5. Parents not willing to place full coverage crowns post-treatment.\n6. Clinical diagnosis of irreversible pulpitis between two adjacent primary molars is not sharply defined.\n7. Unable to perform clinical procedure under rubber dam",true,"4 Years","9 Years",{"count":53,"type":21},80,[24],"This randomised controlled trial aims to compare treatment outcomes between pulpotomy and pulpectomy when used to treat vital primary molars diagnosed with symptomatic irreversible pulpitis. Compared to the standard pulpectomy treatment, pulpotomy is a technically simpler procedure, less time consuming, easier for young patients to tolerate, while retaining the proprioceptive sensation of the tooth - all important advantages when treating young children.",[57],"Irreversible Pulpitis",[59,60,61,62],"Pulpectomy","Pulpotomy","Vital primary molars","Irreversible pulpitis","NOT_YET_RECRUITING","2025-04-08",{"date":66,"type":34},"2025-04-11",{"date":68,"type":21},"2025-07-01",{"date":70,"type":21},"2028-06-30",{"name":40,"class":41},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":80,"minAge":18,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":85,"conditions":86,"keywords":90,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":4},"100546950","outcomes-after-unified-versus-standard-gdm-diagnosis-100546950","NCT06401629","Outcomes After Unified Versus Standard GDM Diagnosis","The UPDATE-GDM Study: OUtcomes After NPRP anD ConventionAl CriTEria for GDM Diagnosis: A Pragmatic Randomised Trial","UPDATE-GDM","Inclusion Criteria:\n\n* This will include broad eligibility criteria of age 18-45 years with or without risk factors at first antenatal care (ANC) visit who are willing to undergo testing at 24-28 weeks and able to provide informed consent.\n\nExclusion Criteria:\n\n* a multiple pregnancy at the time of screening, pre-existing diabetes (T1DM, T2DM)\n* any medical condition affecting glucose metabolism or the results of the GTT (e.g., Cushing's syndrome, bariatric surgery history)\n* known history of major conditions that could interfere with the study or pregnancy outcomes (e.g., severe liver, renal or cardiovascular disorders, chronic infections).","FEMALE","45 Years",{"count":83,"type":21},2650,[24],"Gestational diabetes mellitus (GDM) is a condition that can affect pregnant women during pregnancy and may cause complications for the mother and the baby. Therefore, early and accurate detection is necessary to provide the woman and the baby with better health outcomes. Currently, the most commonly used criteria to detect GDM is the International Association of Diabetes and Pregnancy Study Groups (IADPSG) criterion. However, there is a suggestion that it results in over-diagnosis of GDM, and newer methods of diagnosis have been proposed. One such proposal is to have more than a binary outcome of assessment of dysglycemia in pregnancy. The investigator group created this criterion known as the National Priorities Research Program (NPRP) criterion. This clinical trial compares the IADPSG to the NPRP criteria in pregnant women in Qatar to determine if this newer method mitigates overdiagnosis and more accurately identifies women at risk of complications.",[87,88,89],"Gestational Diabetes","Diagnosis","Pregnancy",[91,92,93,94,95,96],"Gestational Diabetes Mellitus","IADPSG","NPRP","Obesity","Dysglycemia","High-risk Pregnancy","2024-05-06",{"date":99,"type":34},"2024-05-08",{"date":101,"type":21},"2025-01-01",{"date":103,"type":21},"2027-06-01",{"name":40,"class":41},""]