[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100530292":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":33,"centralContacts":38,"locations":44,"responsibleParty":61,"collaborators":63,"id":66,"slug":67,"hasResults":68,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":68,"sex":74,"minAge":75,"maxAge":26,"enrollmentInfo":76,"targetDuration":26,"studyType":79,"phases":80,"briefSummary":82,"conditions":83,"keywords":86,"overallStatus":47,"whyStopped":26,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},{"fullName":5,"class":6},"Centre Hospitalier de Valence","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"A control group","ACTIVE_COMPARATOR","Patients will receive standard care, recommendations on physical activity.\n\npatients should wear the wristband continuously for 7 days prior to scheduled hospital visit T0, T1, T2, T3, T4, T5",[13,14],"Behavioral: behavioral","Other: Sedentary",{"label":16,"type":17,"description":18,"interventionNames":19},"B experimental Group","EXPERIMENTAL","1 or 2 physical activity sessions per week, either face-to-face or by videoconference at patient convenience: low-to-moderate intensity aerobic and anaerobic muscle-strengthening session and a 40-minute stretching\u002Fyoga session.\n\npatients should wear the wristband continuously for 7 days prior to scheduled hospital visit T0, T1, T2, T3, T4, T5",[13,14],[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","behavioral","International Physical Activity (IPAQ) Questionnaire, Quality of Life Questionnaire QLQ-C30, HN 43 questionnaire, Multidimensional Fatigue Inventory (MFI) Questionnaire, Big Five Inventory Questionnaire, illness Identity Questionnaire,",[9,16],null,{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"Sedentary","Actimetry (cumulative time without movement over 24h, prolonged sedentary periods \\>30 min without movement. Continuous recording 7 days prior to visit T0, T1, T2, T3, T4, T5",[9,16],[32],"Physical Activity level",[34],{"name":35,"affiliation":36,"role":37},"Guillaume Guillaume","CH VALENCE","PRINCIPAL_INVESTIGATOR",[39],{"name":40,"role":41,"phone":42,"phoneExt":26,"email":43},"Guillaume Buiret","CONTACT","+33475752555","gbuiret@ch-valence.fr",[45],{"facility":46,"status":47,"city":48,"state":26,"zip":49,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"Ch Valence","RECRUITING","Valence","26000","France","FR",{"type":53,"coordinates":54},"Point",[55,56],4.90956,44.9256,{"lat":56,"lon":55},[59],{"name":60,"role":41,"phone":26,"phoneExt":26,"email":43},"Guillaume BUIRET, PHD",{"type":62,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR",[64],{"name":65,"class":6},"Claude Bernard University","100530292","effect-of-physical-activity-program-on-sedentary-of-patients-with-upper-aerodigestive-tract-cancer-100530292",false,"NCT06184880","Effect of Physical Activity Program on Sedentary of Patients With Upper Aerodigestive Tract Cancer","Effect of Physical Activity Program on Sedentary and Physical Activity Level of Patients With Upper Aerodigestive Tract Cancer","APAORL2","Inclusion Criteria:\n\n* Patients ≥18 years\n* newly diagnosed, histologically proven Upper Aerodigestive Tract Cancer, non-metastatic,\n* life expectancy ≥18 months\n* having a smartphone, tablet or computer with an internet connection enabling remote physical Activity sessions for the experimental group\n\nExclusion Criteria:\n\n* Presenting a contraindication to moderate physical activity\n* Deprived of their liberty by court or administrative decision\n* Unable to be followed for medical, social, family, geographic or psychological reasons for the duration of the study,","ALL","18 Years",{"count":77,"type":78},96,"ESTIMATED","INTERVENTIONAL",[81],"NA","APAORL2 study aims to evaluate the efficacy of a physical activity program on the sedentary and physical activity level during the 18-month program.\n\nAPAORL2 study is a randomized, open label, controlled, monocentric, intervention study that will be conducted among 96 patients treated for localized upper aerodigestive tract cancer.",[84,85],"Upper Aerodigestive Tract Cancer","Head and Neck Cancer",[87,88],"Physical Activity","head and neck cancer","2026-03-17",{"date":91,"type":92},"2026-03-19","ACTUAL",{"date":94,"type":92},"2024-03-19",{"date":96,"type":78},"2029-10-01",{"name":5,"class":6},1]