[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100570807":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":28,"locations":25,"responsibleParty":34,"collaborators":36,"id":40,"slug":41,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":42,"sex":48,"minAge":49,"maxAge":25,"enrollmentInfo":50,"targetDuration":25,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":69,"whyStopped":25,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":25},{"fullName":5,"class":6},"Radboud University Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention group","EXPERIMENTAL","An individualized exercise program consisting of aerobic exercises, strength exercises and balance exercises. The exercises will be prescribed via the Physitrack app.",[13],"Behavioral: Personalised Exercise",{"label":15,"type":16,"description":17,"interventionNames":18},"Historical control group","ACTIVE_COMPARATOR","Aerobic training (see study Voet 2024, Both aerobic exercise and cognitive-behavioral therapy reduce chronic fatigue in FSHD)",[19],"Behavioral: Historical control group",[21,26],{"type":22,"name":23,"description":11,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Personalised Exercise",[9],null,{"type":22,"name":15,"description":17,"armGroupLabels":27,"otherNames":25},[15],[29],{"name":30,"role":31,"phone":32,"phoneExt":25,"email":33},"Ronne van Haaren - Pater","CONTACT","+31 24 36 68 195","Ronne.vanHaaren@radboudumc.nl",{"type":35,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR",[37],{"name":38,"class":39},"Università di Pavia","UNKNOWN","100570807","testing-a-tailored-home-exercise-program-to-reduce-pain-and-fatigue-in-patients-with-fshd-100570807",false,"NCT06712043","Testing a Tailored Home Exercise Program to Reduce Pain and Fatigue in Patients with FSHD.","Testing a Tailored Home Exercise Program to Gain Insight Into Performance Fatigability and Reduce Pain and Fatigue in Patients with FSHD: the GRIP on FSHD Study","GRIPonFSHD","Inclusion Criteria:\n\n* Age \\>18 years\n* Verified diagnosis of FSHD type 1, based on the clinical criteria established by Padberg et al. (1991) (22).\n* Category A or B of the four clinical categories according to the Comprehensive Clinical Evaluation Form (23), these patients have the most peculiar signs of the disease\n* A CIS-fatigue score of ≥ 35\n* Owning of and being able to use a smartphone\n* Preserved ability to ambulate at the time of the selection\n* No pulmonary or cardiological involvement, that could interfere with physical training.\n* Absence of central or peripheral nervous system involvement as from neurological history and physical assessment\n* Absence of limb contractures and tendon retractions\n\nExclusion Criteria:\n\n* Use of beta-blocker medication\n* Presence of additional diseases likely to interfere with the measurements\n* Psychological-psychiatric disorders\n* A musculoskeletal injury that impairs exercising\n* Scoliosis that impairs training\n* Recent adjustment of any medications or medications that may impact fatigue or taking stimulants for fatigue (e.g., Modafinil, amantadine)\n* Current participation in another clinical investigation of a medical device or a drug; or has participated in such a study within 30 days prior to this study\n* Pregnant women\n* Patient incapable of understanding the purpose and conditions of the study, incapable of giving consent or using the app\n* Patient deprived of liberty or patient under guardianship","ALL","18 Years",{"count":51,"type":52},50,"ESTIMATED","INTERVENTIONAL",[55],"NA","The goal of this intervention study is to determine the effect of a tailored exercise program (with aerobic, strength and balance training) in patients with FSHD.\n\nThe main aim is to determine the effect of the exercise program on pain and fatigue.\n\nParticipants will follow a 16 week training program with tailored exercises. The exercises will be prescribed via the app 'Physitrack'. After 16 weeks, the effect on pain, fatigue, fatigability, aerobic capacity, balance, physical function, sleep and the ability to participate in social activities will be determined.",[58],"FSHD",[60,61,62,63,64,65,66,67,68],"Personalized exercise","Rehabilitation","Aerobic exercise","Strength training","Balance training","Fatigue","Pain","Fatigability","Smartphone application","NOT_YET_RECRUITING","2024-11-26",{"date":72,"type":73},"2024-12-02","ACTUAL",{"date":75,"type":52},"2025-02",{"date":77,"type":52},"2025-07",{"name":5,"class":6}]