Quality of Life Clinical Trial
Official title:
Effect of an Exercise Training Intervention on Health-related Quality of Life and Psychosocial and Behavioral Variables in Adult Solid Organ Transplant Recipients: a Quasi-experimental Study Design
The primary aim is to evaluate the short- and long-term effect of the 'Transplantoux' exercise training intervention in solid organ transplant recipients with matched control sample of transplant recipients in view of selected Patient Reported Outcomes (PRO), i.e. health-related quality-of-life (HRQOL), psychosocial and behavioral variables, using a quasi-experimental design.
During the last decades advances in solid organ transplantation, like e.g. organ
preservation, surgical techniques and immunosuppressive treatment have contributed to
improvements in postoperative survival. Thereby, solid organ transplantation (Tx) has moved
from experimental treatment towards a clinical reality and a life-saving surgery, offering
most patients a good long-term survival. However, further improvement in long-term survival
remains a major challenge.
It is increasingly recognized that non-pharmacological interventions hold the potential to
improve long-term outcomes in transplantation as evidence shows that health behavior has
been independently associated with transplant outcome (e.g. physical activity, non-smoking,
medication adherence). Furthermore, exercise training interventions show positive outcome in
a number of populations and limited research in transplantation shows positive outcomes in
view of exercise capacity, muscle strength, cardiopulmonary variables and body composition.
However, there is a lack of research that evaluates exercise training interventions in view
of patient reported outcomes (PROs) in transplant recipients.
In the University Hospitals of Leuven (Belgium) a project named 'Transplantoux' has been
launched to enhance physical activity and exercise capacity in transplant recipients.
Transplant recipients participate in the 'Transplantoux' exercise training intervention for
6-months with the ultimate goal to cycle or hike up the Mont Ventoux (France) (distance:
25.9 km, mean slope: 4.4%). Extending on a previous safety feasibility study in which we
demonstrated that selected Transplant recipients can safely participate in an intense
exercise program and that exercise capacity was significantly improved after training. The
primary aim of the current study is to evaluate the short- and long-term effect of the
'Transplantoux' intervention in view of selected Patient Reported Outcomes (PROs), i.e.
perceived health-related quality-of-life, depressive symptomatology, stress and well-being,
physical activity, social contacts and social support, and barriers and motivators to
exercise.
The Transplantoux Health Evaluation Study (THES) uses a quasi-experimental design with three
convenience samples: 1) a convenience sample of solid organ transplant (Tx)-recipients
participating in the Transplantoux exercise training intervention, 2) matched control sample
of Tx-recipients not participating in the Transplantoux exercise intervention, and 3) and a
convenience sample of healthy controls participating in the Transplantoux exercise
intervention. Selected PROs will be assessed using validated self-reported questionnaire.
Data collection will be performed at baseline, 3 months (in the middle of the training
intervention), 6 months (immediately following the intervention), 9 months (3 months
follow-up period) and 12 months (6 months follow-up period).
;
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor)
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