[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100590802":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":29,"locations":39,"responsibleParty":56,"collaborators":61,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":26,"eligibilityCriteria":69,"healthyVolunteers":70,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":26,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":26,"overallStatus":42,"whyStopped":26,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Local Health Unit Barcelos\u002FEsposende, Public Health Unit","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Interventional Group","EXPERIMENTAL","The interventional group will be subjected to interventions to increase the adherence to screening, including text messages via phone as well as phone calls.",[13],"Other: Arm1: intervention 1 (SMS+call)",{"label":15,"type":16,"description":17,"interventionNames":18},"Control group","PLACEBO_COMPARATOR","The control group will not be subjected to any interventions to increase the adherence to screening.",[19],"Other: Control group",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"OTHER","Arm1: intervention 1 (SMS+call)","The intervention will consist in two text messages (one and two weeks after received the screening test, respectively), an automated non-human call or a call made by the administrative assistant (three weeks after received the screening test), and a phone call made by a physician (four weeks after received the screening test)",[9],null,{"type":22,"name":15,"description":17,"armGroupLabels":28,"otherNames":26},[15],[30,35],{"name":31,"role":32,"phone":33,"phoneExt":26,"email":34},"Marina Barroso Pinheiro MD, PhD, PhD","CONTACT","+351962654712","mpinheiro@icbas.up.pt",{"name":36,"role":32,"phone":37,"phoneExt":26,"email":38},"David Nascimento Moreira MD, Master","+351962692301","dnmoreira@ulsbe.min-saude.pt",[40],{"facility":41,"status":42,"city":43,"state":26,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Public Health Unit Barcelos\u002FEsposende","RECRUITING","Porto","4051-401","Portugal","PT",{"type":48,"coordinates":49},"Point",[50,51],-8.61097,41.1485,{"lat":51,"lon":50},[54],{"name":55,"role":32,"phone":33,"phoneExt":26,"email":34},"Marina Pinheiro MD, PhD, PhD",{"type":57,"investigatorFullName":58,"investigatorTitle":59,"investigatorAffiliation":60,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","David Nascimento Moreira","Public Health Medical Doctor, Local Health Authority","Instituto de Saude Publica da Universidade do Porto",[62],{"name":60,"class":22},"100590802","intervention-project-to-increase-adherence-to-colorectal-cancer-screening-in-barcelosesposende-100590802",false,"NCT06972160","Intervention Project to Increase Adherence to Colorectal Cancer Screening in Barcelos\u002FEsposende","Interventions to Increase Adherence to Colorectal Cancer Screening in Barcelos\u002FEsposende: a Randomized Clinical Trial","Inclusion Criteria:\n\nParticipants must be registered in the ULS of\n\nBarcelos\u002FEsposende and meet the following criteria:\n\n1. Age between 50 and 74 years.\n2. No symptoms such as weight loss in the last 6 months or gastrointestinal symptoms.\n3. No prior diagnosis of CRC.\n4. No diagnosis of inflammatory bowel disease (ulcerative colitis or Crohn's disease).\n5. No family history of CRC in first- and second-degree relatives diagnosed before age 60.\n6. No prior fecal occult blood test (FOBT) in the 11 months before receiving the collection kit or no prior sigmoidoscopy or colonoscopy in the last 24 months.\n\nExclusion Criteria:\n\n1. Participants who did not receive the screening kit at home.\n2. Participants without a phone number.\n3. Participants who do not answer the phone or refuse to participate in the study.\n4. Participants unable to consent or perform the screening due to physical, mental, or other conditions that seriously impair comprehension.",true,"ALL","49 Years","75 Years",{"count":75,"type":76},1038,"ESTIMATED","INTERVENTIONAL",[79],"NA","An experimental study through a randomized clinical trial, without blinding (for participants and the research team), with a control group (not subject to intervention) and an intervention group (subject to two text messages, an automated non-human call or a call made by the administrative assistant, and a phone call made by a physician).",[82],"Colon and Rectal Cancer","2025-05-06",{"date":85,"type":86},"2025-05-14","ACTUAL",{"date":88,"type":86},"2025-04-01",{"date":90,"type":76},"2025-12-31",{"name":5,"class":6},1]