MedPath

"When Movement Moves" - The Health Benefits Among Individuals With Low Physical Mobility Moved by Others

Not Applicable
Completed
Conditions
Physical Disability
Healthy
Interventions
Other: Training in the local departments of TT and cycling trips with CUA
Registration Number
NCT04536779
Lead Sponsor
University of Southern Denmark
Brief Summary

The purpose of the trial is to investigate the physiological, mental, social health effect among individuals with low physical mobility participating in one of the two pre-existing initiatives: the Danish 'Team Twin' and Cycling Without Age. In these, the individuals with low physical mobility are moved by and together with by normal functioning volunteers.

Based on the above, this research project will answer the following research questions:

1. Does movement by others improves the quality of life (QOL) among individuals with low physical mobility

2. Does movement by others improves the physiological health among individuals with low physical mobility

3. Does moving individuals with low physical mobility improve health among normal functioning individuals (i.e volunteer runners and pilots)?

4. How does participation in the physical activity initiatives influence well-being, relations and attitudes among relatives (to the disabled individuals) and employees at nursing homes?

Detailed Description

The research project consists of two sub-projects, where data collection will take place independently of each other. For both projects, we will use a self-controlled study design with pre- and post-measurements of the participant. Through a mixed-method design combining both quantitative and qualitative data will be obtained from the following three target groups:

1. Individuals with low physical mobility (referred to as 'Handiathletes' in the TT-subproject and 'Passengers' in the CUA-sub project)

2. Volunteers (Runners and Pilots)

3. Relatives (to the Handiathletes) and employees at nursing homes (older people)

I collaboration with the two initiatives: the Team Twin- \& Cycling without Age-foundation, the study intend to recruit approximately 25 'Handiathletes' and 25 'Passengers' with low physical mobility and a non-defined number of volunteer-runners, pilots and relatives from most recent established local departments of TT and nursing homes who offers the CUA-concepts to the nursing home residents. Prior to the enrollment, all participants will be given oral and written participant information and give their written consent to participate. Depending on the target group, each group will undergo different data collection methods (described under outcome).

Team Twin description:

Primo 2021, the Handiathletes (TT) who meet eligibility criteria will undergo two clinical pre-test days within a two weeks interval. Starting from approximately ultimo February, a training period of minimum 3 months will start. All the participant target groups train and participate in prescheduled races in their respective departments of TT. During the 3 months of training, data will be collected from the different target groups (see outcome measure). After the 3 months of training, the 'Handiathletes' will undergo one clinical post-test.

The Cycling Without Age description:

Primo 2021, the Pilots (CUA) who meet eligibility criteria will be enrolled in the project - a trial period of minimum 3 months. We will conduct pre- and post measures regarding the research questions (described under outcome)

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
76
Inclusion Criteria

Disabled from the departments of TT:

  • Pass the medical examination conducted by the responsible investigator at the laboratory.

Volunteers;

  • Active member of a local department of TT
  • Volunteer in Cycling without Age

Relatives and nursing home employees;

  • Relative to the enrolled disabled participant
  • working at a nursing home who offers CUA
Exclusion Criteria
  • Sustain damage, which makes the person unable to continue the training sessions.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Individuals with low mobility (Disabled and Elder)Training in the local departments of TT and cycling trips with CUAminimum 8-10 training sessions in at least three months.
Primary Outcome Measures
NameTimeMethod
Quality Of Life (QOL)Baseline to follow-up

Validated self-reported measure of quality of life (i.e. Cantril Ladder)

Secondary Outcome Measures
NameTimeMethod
AutonomyBaseline to follow-up

Measured by interviews and self-reported questionnaire:

* Independence in activities of daily living

* Feeling of being in control of and taking act in one's own life

* options and choices

Social HealthBaseline to follow-up

Measured by interviews and self-reported questionnaire:

* Network, relations and Sense of Coherence (SOC)

* Acceptance from surroundings

Physiological HealthBaseline to follow-up

Measured objectively and by self-report:

* Cardiorespiratory and metabolic fitness

* Cognitive and physical functioning

* Quantity and severity of symptoms related to their disease/disability

* Sleep quality and duration

Mental HealthBaseline to follow-up

Measured by self-reported questionnaire and interviews:

* wellbeing and life satisfaction

* loneliness

* Acceptance and coping (learn to live with diagnosis)

Trial Locations

Locations (1)

National institute of Public Health

🇩🇰

Copenhagen, Denmark

© Copyright 2025. All Rights Reserved by MedPath