Prehabilitation for Gastrectomy
-
- STATUS
- Recruiting
-
- participants needed
- 128
-
- sponsor
- National Cancer Institute, Lithuania
Summary
Description
This study will investigate personalized trimodal
Patients will undergo 6 Minutes Walking Test (6-MWT), spiroergometry (VO2 max; AT), a grip
strength test, a timed Up & Go (TUG) test, 10 m sprint test and sit to stand test before and
after
- Nutritional intervention: The dietetic physician will perform physical examination and
evaluation of the nutritional status to provide individualized care to each patient.
Patients will receive personalized recommendations for the prevention or correction of
malnutrition . - Psychological intervention: Patients will undergo consultation by specialized
onco-psychologist. The
anxiety anddepression level will be evaluated by HAD score and patients will be trained to perform techniques, such as relaxation to reduce and manageanxiety on at home basis.
The psychologist also will enhance patients' motivation to comply with the exercise and nutritional aspects of the intervention.
3. Exercise intervention: Patients will be consulted by PM&R physicians and physiotherapists and personalized exercise plans will be developed according to the results of 6MWT, AT and VO2peak. Exercises will focus on skeletal muscles and cardiopulmonary function training and the exercises feasible at home basis will be selected. All patients will undergo three supervised training sessions to learn the correct exercise techniques.
All patients will be routinely contacted to ensure compliance with
Patients scheduled for
Control group:
Patients will also undergo 6 Minutes Walking Test (6-MWT), spiroergometry (VO2 max; AT), a
grip strength test, a timed Up & Go (TUG) test, 10 m sprint test and sit to stand test before
Details
Condition |
Gastropathy, |
---|---|
Age | 18years - 100years |
Treatment |
|
NCT04223401 | |
Sponsor | National |
Last Modified on | 19 February 2024 |
How to participate?
,
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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