Ignite Creation Date:
2024-05-19 @ 5:34 PM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06411756
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-07-03
First Post:
2024-05-06
Brief Title:
Physical Activity Centers Empowerment
Sponsor:
UNC Lineberger Comprehensive Cancer Center
Organization:
UNC Lineberger Comprehensive Cancer Center
Study Overview
Official Title:
Physical Activity Intervention Co-created and Tested With African American Colorectal Cancer Survivors
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PACE
Brief Summary:
This research study tests the feasibility of the Physical Activity Centers Empowerment PACE physical activity intervention for African American individuals diagnosed with colorectal cancer
Feasibility will be measured as intervention reach effectiveness adoption implementation and maintenance Seventy-two subjects will be recruited to conduct a pilot two-group randomized repeated measures study
Feasibility will be measured as intervention reach effectiveness adoption implementation and maintenance Seventy-two subjects will be recruited to conduct a pilot two-group randomized repeated measures study
Detailed Description:
The purpose of this research is to improve the quality of life for underserved cancer survivors by increasing physical activity A physical activity intervention will be tested for feasibility with African American cancer survivors The project will serve as a foundation for intervening with other underserved cancer survivors
Feasibility will be measured as intervention Reach Effectiveness Adoption Implementation and Maintenance following the RE-AIM framework Survey and biomarker data will be collected at baseline 3 and 9 months later These time points will facilitate exploration of changes pre- and post-intervention and to determine if effects are maintained 6 months after completing the intervention Our primary hypothesis is that the intervention will be feasible to deliver
Feasibility will be measured as intervention Reach Effectiveness Adoption Implementation and Maintenance following the RE-AIM framework Survey and biomarker data will be collected at baseline 3 and 9 months later These time points will facilitate exploration of changes pre- and post-intervention and to determine if effects are maintained 6 months after completing the intervention Our primary hypothesis is that the intervention will be feasible to deliver
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 1K23MD015719-01 | NIH | None | httpsreporternihgovquickSearch1K23MD015719-01 |