- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03898492
Quality Assessment of a Training Period for Physical and Mentally Disabled People
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study aimed at making a quality assessment of a 8 week training period for adults with physical and mental disabilities. A control group was added to compare the effect of the training with no training. Before the training period the participants were tested in relation to their physical status: weight, height, fat%, blood pressure, Aastrand test, chair stand test and waist circumference. In addition to this, the participants were instructed to wear an accelerometer to measure step and active minutes for 2-3 days a work.
The staff at the day center, where the participants works in daytime, were responsible for the physical training 2 times/week for 8 weeks. The training was an hour of combined aerobic, strength, balance and flexibility training.
The participants were tested after the training period using the same test-protocol as before.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
-
Aalborg, Danmark, 9220
- Department of Physiotherapy, University College of Northern Jutland
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- User of the centers included in the study
- Being able to stand alone
- Being able to use an exercise bike
- Being able to understand danish
Exclusion Criteria:
- Pregnancy
- Pacemaker
- Not being able to stand up by themselves
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Andet: Intervention
The participants in this group participated in exercise two times/week for 8 weeks
|
Training two times/week for an hour each time in 8 weeks.
The training included strength training, aerobic training, balance training and flexibility training.
The training was modified to the participants and initiated by the staff at the center.
|
Ingen indgriben: Control
The participants in the control group were instructed to maintain their daily routines.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Body mass index
Tidsramme: Through study completion, an average of 8 weeks
|
weight (kg)/height (m) x height (m)
|
Through study completion, an average of 8 weeks
|
Blood pressure
Tidsramme: Through study completion, an average of 8 weeks
|
Diastolic pressure (mmHg) Systolic pressure (mmHg)
|
Through study completion, an average of 8 weeks
|
Completed chair stands
Tidsramme: Through study completion, an average of 8 weeks
|
Number of completed chair stands
|
Through study completion, an average of 8 weeks
|
Aastrand test
Tidsramme: Through study completion, an average of 8 weeks
|
Bike test to measure the physical fitness.
|
Through study completion, an average of 8 weeks
|
Waist circumference
Tidsramme: Through study completion, an average of 8 weeks
|
Measured in cm
|
Through study completion, an average of 8 weeks
|
Physical activity
Tidsramme: During test session - 2-3 days
|
Number of steps and active minutes
|
During test session - 2-3 days
|
Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Studieleder: Dorte Drachmann, Msc, University College of Northern Jutland, Denmark. Department of Physiotherapy
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- FOU-UU-2018-001
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Physical training
-
Florida State UniversityOhio State University; Ohio UniversityRekrutteringDemens | Angst | Alzheimers sygdom | Mild kognitiv svækkelseForenede Stater
-
University of Texas Southwestern Medical CenterTilmelding efter invitation
-
Guohua ZengUkendt
-
Gaziosmanpasa Research and Education HospitalAfsluttetCovid19 | Post-intensiv afdelings syndromKalkun
-
Saglik Bilimleri UniversitesiMedical Park Hospital IstanbulAfsluttetICU patienter | ICU erhvervet svaghedKalkun
-
Wake Forest University Health SciencesNational Heart, Lung, and Blood Institute (NHLBI)AfsluttetFysisk aktivitetForenede Stater
-
University of Massachusetts, WorcesterEunice Kennedy Shriver National Institute of Child Health and Human Development... og andre samarbejdspartnereAfsluttet
-
Hasselt UniversityTel Aviv University; Sheba Medical Center; Centre Hospitalier Universitaire... og andre samarbejdspartnereAfsluttet
-
Yale UniversityAfsluttetPsykisk helbredsproblem (f.eks. depression, psykose, personlighedsforstyrrelse, stofmisbrug) | Mental sundhed velvære 1 | Krigsrelateret traumeJordan