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Quality Assessment of a Training Period for Physical and Mentally Disabled People

Quality Assessment of a Training Period for Physical and Mentally Disabled People

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03898492
Enrollment
23
Registered
2019-04-02
Start date
2018-01-03
Completion date
2018-05-31
Last updated
2019-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disabled Persons, Exercise

Brief summary

The aim of the study was to evaluate the effect of a 8 week training period compared with control group in physical and mentally disabled adults. The effect was evaluated in relation to their physical status. Furthermore, physical activity was measured using steps and active minutes.

Detailed description

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.

Interventions

OTHERPhysical training

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.

Sponsors

TRYG Foundation
CollaboratorOTHER
University College of Northern Denmark
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

One intervention group and one control group

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Body mass indexThrough study completion, an average of 8 weeksweight (kg)/height (m) x height (m)
Blood pressureThrough study completion, an average of 8 weeksDiastolic pressure (mmHg) Systolic pressure (mmHg)
Completed chair standsThrough study completion, an average of 8 weeksNumber of completed chair stands
Aastrand testThrough study completion, an average of 8 weeksBike test to measure the physical fitness.
Waist circumferenceThrough study completion, an average of 8 weeksMeasured in cm
Physical activityDuring test session - 2-3 daysNumber of steps and active minutes

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026