- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02729883
Take the Fight in Supporting and Empowering Patients With Cancer
A Pilot Study of 'Take the Fight' as Community-Based Participatory Research
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
PRIMARY OBJECTIVES:
I. Delineate the benefits of and limitations to having Take the Fight strategists, performing as lay-navigators, as perceived by both the patients and the students.
SECONDARY OBJECTIVES:
I. Investigate changes in self-reported outcomes for patients and the Take the Fight strategists.
OUTLINE:
Patients receive patient navigation via strategists from the Take the Fight for 8 weeks. Patients also complete interviews regarding perceived physical, logistical, psychosocial, and informational challenges experienced prior to meeting with strategists/navigators and how challenges were addressed by navigator or others, perceived benefits or limitations of navigator assistance. Strategists also complete interviews regarding their perceptions on how patients benefited from participation, challenges patients experienced that were directly or indirectly related to their cancer diagnosis and treatment, how these concerns were addressed, barriers to addressing these concerns, and patient health literacy.
After completion of study, patients and strategists are followed up for 8-10 weeks.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
North Carolina
-
Winston-Salem, North Carolina, Forenede Stater, 27157
- Comprehensive Cancer Center of Wake Forest University
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- PATIENTS ELIGIBILITY CRITERIA
- Have histologically confirmed cancer
- Karnofsky performance scale (KPS) score of >= 60
- The ability to understand and be willing to sign an informed consent document
- Willing to undergo a form of cancer therapy and subsequent follow-up care
- STRATEGISTS INCLUSION CRITERIA
- Age >= 18 years
- Wake Forest University student
- Have volunteered as a student strategist at Comprehensive Cancer Center of Wake Forest University (CCCWFU); all strategists are required to have gone through Take the Fight (TTF) training prior to their volunteer work
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Supportive care (Take the Fight)
Patients receive patient navigation via strategists from the Take the Fight for 8 weeks.
Patients also complete interviews regarding perceived physical, logistical, psychosocial, and informational challenges experienced prior to meeting with strategists/navigators and how challenges were addressed by navigator or others, perceived benefits or limitations of navigator assistance.
Strategists also complete interviews regarding their perceptions on how patients benefited from participation, challenges patients experienced that were directly or indirectly related to their cancer diagnosis and treatment, how these concerns were addressed, barriers to addressing these concerns, and patient health literacy.
|
Hjælpestudier
Andre navne:
Complete interviews
Receive patient navigation via the Take the Fight strategists
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in patients self-reported outcomes using European Organization for Research and Treatment of Cancer (EORTC) Quality of Life-Cancer 30 (QLQ-C30) questionnaire
Tidsramme: Baseline to up to 18 weeks
|
Descriptive statistics will be measured, including frequencies, percentages, means and standard deviations of patient self-report measures will be calculated.
Ninety-five percent confidence intervals will also be calculated for the outcomes measures at each time point.
|
Baseline to up to 18 weeks
|
|
Change in strategists self-reported outcomes using Caregiver Quality of Life Index-Cancer (CQOLC, McMillian, 1996) scale
Tidsramme: Baseline to up to 10 weeks
|
Baseline to up to 10 weeks
|
Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Stefan Grant, Wake Forest University Health Sciences
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- IRB00037093
- P30CA012197 (U.S. NIH-bevilling/kontrakt)
- NCI-2016-00384 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
- CCCWFU 99216 (Anden identifikator: Comprehensive Cancer Center of Wake Forest University)
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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