- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03898492
Quality Assessment of a Training Period for Physical and Mentally Disabled People
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
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Aalborg, Danmark, 9220
- Department of Physiotherapy, University College of Northern Jutland
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
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
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Övrig: 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.
|
Inget ingripande: Control
The participants in the control group were instructed to maintain their daily routines.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Body mass index
Tidsram: 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
Tidsram: 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
Tidsram: Through study completion, an average of 8 weeks
|
Number of completed chair stands
|
Through study completion, an average of 8 weeks
|
Aastrand test
Tidsram: Through study completion, an average of 8 weeks
|
Bike test to measure the physical fitness.
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Through study completion, an average of 8 weeks
|
Waist circumference
Tidsram: Through study completion, an average of 8 weeks
|
Measured in cm
|
Through study completion, an average of 8 weeks
|
Physical activity
Tidsram: During test session - 2-3 days
|
Number of steps and active minutes
|
During test session - 2-3 days
|
Samarbetspartners och utredare
Samarbetspartners
Utredare
- Studierektor: Dorte Drachmann, Msc, University College of Northern Jutland, Denmark. Department of Physiotherapy
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- FOU-UU-2018-001
Läkemedels- och apparatinformation, studiedokument
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