This study aims to investigate the effectiveness of a multicomponent intervention in promoting physical activity among adults with ID.
ID
Source
Brief title
Condition
- Psychiatric and behavioural symptoms NEC
- Lifestyle issues
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The primary study parameter is the difference in physical activity of the
adults with ID.
Secondary outcome
For adults with ID:
Level of functioning
- Activities of Daily Living (ADL) and Instrumental Activities of Daily Living
(IADL): Barthel Index and the Lawton IADL scale.
- Mobility level (required use of aids)
-Health status
Level of problem behavior
Personal attitude of adults with ID towards physical activity behavior: stage
of change, attitude towards physical activity, barriers to change, fear of
falling, pain, previous physical activity experiences of the participant,
preferences and desires regarding physical activity, preferences and/or desire
to explore regular exercise facilities or activities in the community.
For primary care givers:
Attitude towards implementing sufficient physical activity in daily care of
care professionals
Stage of change to implement sufficient physical activity and barriers to
change
Background summary
Physical activity levels are very low in adults with intellectual disabilities
(ID), and physical activity promotion for the general population is not
feasible in this group, due to the specific characteristics of adults with ID
and specific characteristics of their support/care setting.
Study objective
This study aims to investigate the effectiveness of a multicomponent
intervention in promoting physical activity among adults with ID.
Study design
Quasi-experimental repeated measures design
Intervention
After a control period of 12 weeks, the entire study sample receives the
12-week intervention which aims at changing behavior of adults with ID
(increase of physical activity) and changing behaviour of primary care givers
(integrate sufficient physical activity in their daily support or care). The
intervention starts with a Quickscan, after which the staff and the clients
participate in an education session about the relevance of physical activity
and possibilities to be active for people with chronic illnesses. The primary
care givers receive advice from a physical activity coach, based on the results
of the Quickscan. After setting goals for 12 weeks, the physical activity coach
continues to coach the primary care givers throughout the process, and visits
the living facility twice to demonstrate easy group activities. Participants
receive a T-shirt with bag at the start, and a medal and certificate at the
end, and the team as a whole collect symbolic euro*s every time a participant
completes a Quickscan.
Study burden and risks
Participants take part in a Quickscan, four times throughout the process of 36
weeks. This Quickscan consists of an interview and low intensity , non-invasive
and painless tasks, except for two submaximal tests. The safety of executing
these two tests is screened on beforehand and checked with a physician in case
of doubt. If safety is not sufficiently confirmed, these two tests are left out
in the Quickscan. Risk of adverse events due to exercise is kept as low as
possible with this procedure. During the Quickscan and the intervention itself,
the individual risk of falling needs to be continuously monitored, as changes
in lifestyle might pose new situations. Furthermore, this intervention takes
the preferences and possibilities of the participants into account when giving
individual advice, which results in a tailored, individual advice. The physical
activity coach advices how to increase physical activity gradually, in small
steps, to prevent injuries or muscle soreness. These small risks do not
outweigh the advantages of a healthy lifestyle, and since this intervention is
designed for adults with ID, this study could not be tested in other
populations.
Westzeedijk 118
Rotterdam 3016 AH
NL
Westzeedijk 118
Rotterdam 3016 AH
NL
Listed location countries
Age
Inclusion criteria
-Age 18 years and over
-Having an intellectual disability
-Receiving residential care from the ID care service Abrona
-Informed consent from participant or legal representative
Exclusion criteria
Severe Illness
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL41410.078.12 |