COMUNICAR: Community-Led Family-Centered Communication for Cancer Survivorship Care
This study will test a novel intervention to facilitate family-centered communication among Hispanic/Latino (H/L) young adult childhood cancer survivors (YA-CCS), their support persons, and their clinicians through collaboration between the clinic and a community-based organization.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Beräknad)
Fas
- Inte tillämpbar
Kontakter och platser
Studiekontakt
- Namn: Stephanie Smith, MD, MPH
- Telefonnummer: 209-609-0208
- E-post: smithsm@stanford.edu
Studieorter
-
-
California
-
Palo Alto, California, Förenta staterna, 94304
- Rekrytering
- Stanford University
-
Kontakt:
- Stephanie Smith, MD, MPH
- Telefonnummer: 209-609-0208
- E-post: smithsm@stanford.edu
-
Huvudutredare:
- Stephanie Smith, MD, MPH
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Childhood cancer survivor previously treated with chemotherapy and/or radiation therapy
- Currently age 18-25 years
- Identifies as Hispanic/Latino
- Currently ≥5 years post cancer diagnosis
- Fluent in English or Spanish
- Receives medical care at Stanford
- Lives within Jacob's Heart service area (zip codes within Monterey, Santa Cruz, Santa Clara, San Benito Counties: https://www.jacobsheart.org/service-area)
- Ability to understand and the willingness to provide written informed consent.
Exclusion Criteria:
1. Lack of proficiency in written and spoken English or Spanish
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Stödjande vård
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Family-Centered Communication
Young Adult Cancer Survivors (YA-CCS)-support person dyads receive a family-centered communication intervention delivered by a community health worker and coordinated around a standard-of-care survivorship clinic visit. |
A novel family-centered communication intervention designed to facilitate communication among Young Adult Cancer Survivors (YA-CCS), their chosen support person, and clinicians through collaboration between the clinic and a community-based organization. The intervention includes pre-visit and post-visit sessions delivered by a community health worker and timed around a standard-of-care survivorship clinic visit. |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Proportion of invited young adult cancer survivor-support person dyads enrolled
Tidsram: From recruitment initiation through completion of study enrollment, up to 24 months
|
Feasibility assessed by the proportion of invited dyads who enroll in the study. |
From recruitment initiation through completion of study enrollment, up to 24 months
|
|
Proportion of enrolled young adult cancer survivors completing all intervention components
Tidsram: From intervention initiation through intervention completion, up to 3 weeks
|
Feasibility assessed by the proportion of enrolled young adult cancer survivor participants who complete all intervention components. |
From intervention initiation through intervention completion, up to 3 weeks
|
|
Mean Theoretical Framework of Acceptability questionnaire score
Tidsram: Post-intervention, within 2 months after intervention completion
|
Acceptability assessed using participant-reported Theoretical Framework of Acceptability (TFA) questionnaire scores. Scores range from 1-5, with higher scores indicating greater acceptability. |
Post-intervention, within 2 months after intervention completion
|
|
Mean Satisfaction With Visit Preparation questionnaire score
Tidsram: Post-intervention, within 2 months after intervention completion
|
Acceptability assessed using participant-reported Satisfaction With Visit Preparation questionnaire scores. Scores range from -10 to 10, with higher scores indicating greater satisfaction. |
Post-intervention, within 2 months after intervention completion
|
Samarbetspartners och utredare
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Stephanie Smith, MD, MPH, Stanford University
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- IRB-85827
- 5K08CA285829 (U.S.S. NIH-anslag/kontrakt)
- NCI-2026-06570 (Registeridentifierare: National Cancer Institute Clinical Trials Reporting Program)
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
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