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

When Movement Moves - A Self-controlled Trial of the Physiological, Mental and Social Health Benefits Among Individuals With Low Physical Mobility Moved by Others in Two Existing Initiatives: the Danish Team Twin and Cycling Without Age

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04536779
Acronym
WMM
Enrollment
76
Registered
2020-09-03
Start date
2021-02-01
Completion date
2022-02-01
Last updated
2023-04-18

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

Conditions

Healthy, Physical Disability

Keywords

non-elite sports community, physically challenged, individuals with low physical mobility, volunteers, relatives, disabled, QOL

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)

Interventions

OTHERTraining in the local departments of TT and cycling trips with CUA

in a minimum of 3 months, the individuals with low physical mobility will conduct a minimum of 8-10 training and cycling sessions.

Sponsors

Rigshospitalet, Denmark
CollaboratorOTHER
Bevica Fonden
CollaboratorOTHER
Sygekassernes Helsefond
CollaboratorOTHER
University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

We will use a study design with pre- and post-measurements. The participant will be their own case-control. For optimizing the statistical strength, the individuals with low mobility will undergo two times of baseline measurements. After a minimum of a three-month trial period followup measurements will be conducted.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Quality Of Life (QOL)Baseline to follow-upValidated self-reported measure of quality of life (i.e. Cantril Ladder)

Secondary

MeasureTime frameDescription
Physiological HealthBaseline to follow-upMeasured 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-upMeasured by self-reported questionnaire and interviews: * wellbeing and life satisfaction * loneliness * Acceptance and coping (learn to live with diagnosis)
Social HealthBaseline to follow-upMeasured by interviews and self-reported questionnaire: * Network, relations and Sense of Coherence (SOC) * Acceptance from surroundings
AutonomyBaseline to follow-upMeasured 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

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026