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Spots Global Cancer Trial Database for Shared Healthcare Actions and Reflections Electronic Systems in Survivorship

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Trial Identification

Brief Title: Shared Healthcare Actions and Reflections Electronic Systems in Survivorship

Official Title: SHARE-S Aim 3: Shared Healthcare Actions & Reflections Electronic Systems in Survivorship

Study ID: NCT04337203

Study Description

Brief Summary: The primary purpose of this study is conduct a pilot study testing the study protocols, implementation program, and mixed-methods data collection.

Detailed Description: Primary Objectives: • To evaluate how successfully SHARE-S can be implemented into clinical care as characterized by rates of enrollment. Investigators hypothesize \>30% of patients e-referred to SHARE-S will enroll. Secondary Objectives: * To assess additional implementation outcomes that evaluate preliminary implementation success (i.e., further assessment of adoption, acceptability, appropriateness, further assessment of feasibility, and fidelity). * To describe service outcome variability to inform future studies. Investigators will assess service outcomes relevant to Commission on Cancer requirements by reporting annual estimates for: (1) the estimated number of patients impacted by SHARE-S; (2) the cancer sites impacted by SHARE-S; and the (3) resources/processes utilized to enhance each of the chosen services if barriers were encountered. We will also assess safety and perceived patient-centeredness of care. * To describe patient health outcome variability to inform future studies (i.e., social role, physical functioning, anxiety, depression, fatigue, sleep disturbance, pain, cancer-specific quality of life, health behaviors, patient autonomy, self-efficacy for managing cancer, engagement with the survivorship care plan document, and satisfaction with care). * To evaluate the Implementation Program we will assess key milestones and processes for this pilot study of the Implementation Stage measured at the clinic level. * To qualitatively assess implementation barriers and facilitators using semi-structured interviews that will be audio-recorded. * To examine how study results vary by cancer type.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, North Carolina, United States

Contact Details

Name: Stephanie Sohl, Ph.D

Affiliation: Wake Forest University Health Sciences

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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