The PreventIT Trial in Young Older Adults, Comparing Two Lifestyle-integrated Exercise Interventions
NCT03065088 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180
Last updated 2019-03-26
Summary
The feasibility randomised controlled trial is part of the EU funded project "PreventIT" (2016-2018) responding to the Horizon 2020, Personalised health and care (PHC), call PHC-21: Advancing active and healthy ageing with ICT: Early risk detection and intervention. The PreventIT project focuses on a new behaviour change activity approach for young older adults (61-70 years of age) with an overall aim of early prevention of functional decline and to empower people to take care of their own health.
Conditions
- Young Older Adults
Interventions
- BEHAVIORAL
-
aLIFE
The aLiFE programme is taught by an instructor during six home visits and 3 phone calls during the 6-month intervention period. The programme will be personalised by use of an initial balance and strength assessment (aLiFE assessment tool). The participants assigns activities to his or her daily activities, and during subsequent home visits, the number of activities and task demands are upgraded. Participants will be taught how to select opportunities themselves to embed activities into their individual daily routine, and how to progress over time.
- BEHAVIORAL
-
eLIFE
The eLIFE includes a personalised ICT-administered training schedule using the activities developed in aLiFE, delivered in the form of video clips, pictures and text/verbal instructions on a smartphone and smartwatch application. Personalisation of activity content will be decided based on a phenotype tool and initial difficulty level is decided through the aLiFE assessment tool. In addition, a virtual instructor teaches the participants how to carry out the eLiFE programme. The user receives motivational messages and feedback, and there will be a possibility for social interaction between the participants. The instructors teach the eLiFE participants the programme during 4 home visits and 3 phone calls during the 6 month intervention period.
- BEHAVIORAL
-
control
The control group follows the World Health Organization's recommendations of physical activity. The control participants will receive one home visit and be given a written letter with the activity recommendations.
Sponsors & Collaborators
-
VU University of Amsterdam
collaborator OTHER -
Robert Bosch Gesellschaft für Medizinische Forschung mbH (RBMF)
collaborator OTHER -
University of Bologna
collaborator OTHER -
University of Manchester
collaborator OTHER -
Local Centre Health Unit Tuscany
collaborator UNKNOWN -
Ecole Polytechnique Fédérale de Lausanne
collaborator OTHER -
Doxee S.p.A.
collaborator UNKNOWN -
Health Leads BV
collaborator UNKNOWN -
Norwegian University of Science and Technology
lead OTHER
Principal Investigators
-
Jorunn Helbostad, phd prof · Norwegian Universitiy of Science and Technology
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 61 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-02-28
- Primary Completion
- 2018-08-31
- Completion
- 2018-08-31
Countries
- Germany
- Netherlands
- Norway
Study Locations
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