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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03898492
Other study ID # FOU-UU-2018-001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 3, 2018
Est. completion date May 31, 2018

Study information

Verified date March 2019
Source University College of Northern Denmark
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date May 31, 2018
Est. primary completion date May 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 64 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Physical 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.

Locations

Country Name City State
Denmark Department of Physiotherapy, University College of Northern Jutland Aalborg

Sponsors (2)

Lead Sponsor Collaborator
University College of Northern Denmark TRYG Foundation

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Body mass index weight (kg)/height (m) x height (m) Through study completion, an average of 8 weeks
Primary Blood pressure Diastolic pressure (mmHg) Systolic pressure (mmHg) Through study completion, an average of 8 weeks
Primary Completed chair stands Number of completed chair stands Through study completion, an average of 8 weeks
Primary Aastrand test Bike test to measure the physical fitness. Through study completion, an average of 8 weeks
Primary Waist circumference Measured in cm Through study completion, an average of 8 weeks
Primary Physical activity Number of steps and active minutes During test session - 2-3 days
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