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

NCT ID: NCT03898492

Last Updated: 2019-04-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

23 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-03

Study Completion Date

2018-05-31

Brief Summary

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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

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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.

Conditions

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Disabled Persons Exercise

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

One intervention group and one control group
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Intervention

The participants in this group participated in exercise two times/week for 8 weeks

Group Type OTHER

Physical training

Intervention Type OTHER

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.

Control

The participants in the control group were instructed to maintain their daily routines.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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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.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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TRYG Foundation

OTHER

Sponsor Role collaborator

University College of Northern Denmark

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dorte Drachmann, Msc

Role: STUDY_DIRECTOR

University College of Northern Jutland, Denmark. Department of Physiotherapy

Locations

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Department of Physiotherapy, University College of Northern Jutland

Aalborg, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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FOU-UU-2018-001

Identifier Type: -

Identifier Source: org_study_id

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