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Trial of Spiritual Care Interventions for Patients With Cancer 288

Ainda não recrutando
Os detalhes do estudo clínico estão disponíveis principalmente em inglês. No entanto, a IA Trial Radar pode ajudar! Basta clicar em 'Explicar o estudo' para visualizar e discutir as informações do estudo no idioma selecionado.
O estudo clínico NCT07408310 é um estudo intervencionista para Câncer avançado. Seu status atual é: ainda não recrutando. O recrutamento está programado para iniciar em 1 de fevereiro de 2026, com o objetivo de incluir 288 participantes. Coordenado por Weill Medical College of Cornell University e deve ser concluído em 1 de junho de 2029. Essas informações foram atualizadas no ClinicalTrials.gov em 13 de fevereiro de 2026.
Resumo
This study aims to determine the effects of 2 spiritual care interventions. Spiritual wellness and healthcare service utilization will be measured from a sample of advanced cancer patients recruited from outpatient settings.
Descrição detalhada
This study is a stratified permuted-block RCT to determine the effects of 2 spiritual care interventions on advanced cancer patients' spiritual wellness (i.e., spiritual well-being and satisfaction of spiritual care needs) and specific forms of healthcare service utilization (i.e., hospice enrollment and ICU admissions) in a sample of advanced cancer patients (N=288) recruited from outpatient settings. Patients will ...Mostrar mais
Título oficial

Trial of Spiritual Care Interventions for Patients With Cancer

Condições médicas
Câncer avançado
Outros IDs do estudo
Número NCT
Data de início (real)
2026-02
Última atualização postada
2026-02-13
Data de conclusão (estimada)
2029-06
Inscrição (estimada)
288
Tipo de estudo
Intervencionista
FASE
N/A
Status
Ainda não recrutando
Palavras-chave
Advanced Cancer
Spiritual Care
Propósito principal
Cuidados de suporte
Alocação do design
Randomizado
Modelo de intervenção
Paralelo
Cegamento (Mascaramento)
Triplo-cego
Braços / Intervenções
Grupo de participantes/BraçoIntervenção/Tratamento
ExperimentalSpiritual Care Intervention #1
This is an experimental condition arm. Intervention details are being withheld until the trial concludes to protect the scientific integrity of the study.
Spiritual Care Intervention #1
Experimental
ExperimentalSpiritual Care Intervention #2
This is also an experimental condition arm. Intervention details are being withheld until the trial concludes to protect the scientific integrity of the study.
Spiritual Care Intervention #2
Experimental
Comparador ativoSpiritual Care Intervention #3
This is the active comparator condition arm. Intervention details are being withheld until the trial concludes to protect the scientific integrity of the study.
Spiritual Care Intervention #3
Active Comparator
Desfecho primário
Medida de desfechoDescrição da medidaPrazo
Patients' spiritual wellness as assessed by measures of spiritual well-being
The spiritual well-being outcome measure for this trial is the total score for the 12-item Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being Scale \[FACIT-Sp-12\], which has a range from 0 to 48. The higher the score, the greater the spiritual well-being.
2 months
Participants' number of hospice enrollments
Number of hospice enrollments over time, up to 12 months.
up to 12 months
Participants' number of ICU admissions
Number of ICU admissions over time, up to 12 months.
up to 12 months
Patients' spiritual wellness as assessed by measures of satisfaction of spiritual care needs.
The satisfaction of spiritual care needs outcome measure for this trial is a reverse-coded total score for the 13-item Spiritual Needs Assessment for Patients \[SNAP\], which measures unmet spiritual care needs and has a range from 13 to 52. The higher the reverse-coded score, the greater the satisfaction of spiritual care needs.
2 months
Desfecho secundário
Medida de desfechoDescrição da medidaPrazo
Patients' quality of life
The quality-of-life outcome measure for this trial is the total score for the 27-item Functional Assessment of Cancer Therapy - General \[FACT-G\], which has a range of 0 to 108. The higher the score, the greater the quality of life.
2 months
Assistente de participação
Critérios de elegibilidade

  1. Diagnosed with an advanced cancer.

  2. Member of a religious faith community organization.

  3. Fluent in English.

  4. Received spiritual care from a healthcare chaplain within the past 2 months.

  5. Too weak or cognitively impaired to engage in study activities.

Weill Medical College of Cornell University logoWeill Medical College of Cornell University
Contato central do estudo
Contato: Madison K Pavao, B.S., (646)962-5650, [email protected]
Contato: Paul K Maciejewski, Ph.D., 646-962-7169, [email protected]
3 Locais do estudo em 1 países

New York

New York Presbyterian Brooklyn Methodist Hospital, New York, New York, 11215, United States
Alan B Astrow, M.D., Contato, (718) 780-5824, [email protected]
Alan B Astrow, M.D., Investigador principal

Texas

The University of Texas Medical Branch, Galveston, Galveston, Texas, 77555, United States
Mukaila Raji, M.D., Contato, (409) 772-1989, [email protected]
Mukaila Raji, M.D., Investigador principal
M.D. Anderson Cancer Center, Houston, Texas, 77030, United States
David Hui, M.D., Contato, (713) 563-7630, [email protected]
David Hui, M.D., Investigador principal