Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06623097
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-30
Brief Title:
Exercise and Nutrition for Older Cancer Survivors and Their Support Person the Vitality Study
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Exercise and Nutrition for Older Cancer Survivors and Their Support Person the Vitality Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
VITALITY
Brief Summary:
This research study will compare the impact of virtually supervised and unsupervised home-based exercise and diet programs on cognitive function and physical function among cancer survivors and support persons This study will involve a 6 month home-based virtually supervised or unsupervised exercise and diet intervention
The names of the study interventions involved in this study are
Virtually supervised exercise and healthy diet care
Unsupervised exercise and healthy diet care
The names of the study interventions involved in this study are
Virtually supervised exercise and healthy diet care
Unsupervised exercise and healthy diet care
Detailed Description:
This is a multi-center parallel arm comparative effectiveness trial to compare the impact of supervised and unsupervised home-based exercise and diet programs on cognitive function and physical function among cancer survivors and support persons
Participants and support persons in this study will be randomly assigned to one of two groups Group A Virtually Supervised Care or Group B Unsupervised Care Randomization means a participant is placed into a study group by chance
The research study procedures include screening for eligibility in-clinic visits evaluations of fitness physical health diet and cognitive function surveys and questionnaires
Participation in this study is expected to last 12 months
It is expected about 1528 people will participate in this research study
Patient Centered Outcomes Research Institute PCORI is supporting this research study by providing funding for the study
Participants and support persons in this study will be randomly assigned to one of two groups Group A Virtually Supervised Care or Group B Unsupervised Care Randomization means a participant is placed into a study group by chance
The research study procedures include screening for eligibility in-clinic visits evaluations of fitness physical health diet and cognitive function surveys and questionnaires
Participation in this study is expected to last 12 months
It is expected about 1528 people will participate in this research study
Patient Centered Outcomes Research Institute PCORI is supporting this research study by providing funding for the study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None