Rural Survivorship Navigation Program (RSVP)
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|ClinicalTrials.gov Identifier: NCT03880526|
Recruitment Status : Recruiting
First Posted : March 19, 2019
Last Update Posted : April 29, 2020
|Condition or disease|
To enhance understanding of the comprehensive psychosocial and medical needs of cancer survivors and caregivers in rural northwest North Carolina, focusing on their health needs, psychosocial concerns, perceived needs related to cancer and survivorship care, access/barriers to care, and knowledge/perceptions of clinical research using focus groups and semi-structured interviews. This aim is hypothesis-generating.
To document rural cancer patient/survivors' reports of: a) health behaviors; b) psychosocial needs; c) current health-related information and supportive care needs; d) barriers to care; e) symptoms and health-related quality of life using a quantitative survey
|Study Type :||Observational|
|Estimated Enrollment :||240 participants|
|Official Title:||Rural Survivorship naVigation Program (RSVP): Building Community Capacity for Cancer Control|
|Actual Study Start Date :||February 3, 2020|
|Estimated Primary Completion Date :||May 2021|
|Estimated Study Completion Date :||May 2021|
Participants will choose to participant in an individual in-depth interview to be conducted by investigators to gain information about the participant's background, cancer status and treatment.
Participants may choose to participate in one of three focus groups of no more than 10 participants in each group to to gain information about the participant's background, cancer status and treatment.
- Improving Cancer-Related Experiences Through Interviews or Focus Group Settings [ Time Frame: 90 minutes ]Through focus groups or interviews information will be collected on participants' experience receiving cancer-related care and to ask for specific suggestions and ways to improve care and cancer-related resources for adults living in a rural area.
- Measurement of Quality of Life [ Time Frame: 90 minutes ]The PROMIS Global 10 survey will be used to document rural cancer patient/survivors' reports of: a) health behaviors; b) psychosocial needs; c) current health-related information and supportive care needs; d) barriers to care; e) symptoms and health-related quality of life using a quantitative survey. Survey scoring consists of 5=Never, 4=Rarely, 3=Sometimes, 2=Often and 1=Always.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03880526
|United States, North Carolina|
|Wake Forest Baptist Comprehensive Cancer Center||Recruiting|
|Winston-Salem, North Carolina, United States, 27157|
|Contact: Study Coordinator 336-713-6910 firstname.lastname@example.org|
|Principal Investigator: Kathryn Weaver, MPH, PhD|
|Principal Investigator:||Kathryn Weaver, MPH, PhD||Wake Forest University Health Sciences|