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Study of Palliative Care Intervention for Advanced Cancer Patients and Their Caregivers -Educate Nurture Advise Before Life Ends (ENABLE III) (ENABLE III)

2 gennaio 2014 aggiornato da: Dartmouth-Hitchcock Medical Center

Early vs. Later Palliative Cancer Care: Clinical and Biobehavioral Outcomes

ENABLE III is a randomized clinical trial that evaluates a phone-based palliative care intervention designed to improve quality of life, mood, and symptom management for patients with an advanced stage cancer and their caregivers.

The primary aims of this clinical trial are to determine whether a palliative care intervention (introduced immediately or 12 weeks after diagnosis) can improve survival, quality of life, mood, symptom intensity and end-of-life care.

Panoramica dello studio

Descrizione dettagliata

In 2008, cancer claimed more than 565,000 American lives -1,500 people a day. Palliative care strives to improve quality of life (QOL) and to prevent "bad deaths" by providing expert, interdisciplinary care to manage the effects of disease and treatment. Effective end-of-life (EOL) care depends upon proactive, patient-centered interventions to prepare patients and families for the challenges of terminal illness. We were able to demonstrate the feasibility and efficacy of a concurrent oncology palliative care (COPC) intervention in improving quality of life and mood in our previous studies ENABLE I and ENABLE II; however, a number of gaps in our knowledge remain.

Patients will be randomized to begin the intervention either immediately or 12 weeks after a new diagnosis of advanced or recurrent cancer. This phone-based intervention consists of: 1) an Advanced Practice Palliative Care Nurse Interventionist instituting 1a) a 6-session manualized patient curriculum- Charting Your Course (CYC), 1b) a 3-session manualized, caregiver curriculum- the Creativity Optimism Planning Expert information (COPE) program, and 1c) on-going patient and caregiver follow up; and 2) Palliative Care Team Comprehensive Assessment & Management.

Tipo di studio

Interventistico

Iscrizione (Anticipato)

360

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • New Hampshire
      • Lebanon, New Hampshire, Stati Uniti, 03756
        • Dartmouth-Hitchcock Medical Center - Lebanon
      • Manchester, New Hampshire, Stati Uniti, 03102
        • Dartmouth-Hitchcock Clinic - Manchester
      • Nashua, New Hampshire, Stati Uniti, 03060
        • St. Joseph Hospital
      • Nashua, New Hampshire, Stati Uniti, 03063
        • Dartmouth-Hitchcock NCCC Nashua
    • Rhode Island
      • Providence, Rhode Island, Stati Uniti, 02908
        • Providence VA Medical Center
    • Vermont
      • Berlin, Vermont, Stati Uniti, 05061
        • Mountainview Medical
      • White River Junction, Vermont, Stati Uniti, 05001
        • Veteran's Administration Hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

INCLUSION CRITERIA FOR PATIENTS:

  1. Able to speak and understand English
  2. Over age 18
  3. NEW diagnosis, recurrence, or progression of an advanced stage cancer within THIRTY days of the date the patient was informed of the diagnosis by his/her oncology clinician.
  4. Estimated survival of 2 years or less
  5. Diagnosed with an advanced stage cancer such as one of the following:

    • Lung Cancer: Stage IIIB or IV non-small cell, or extensive stage small cell
    • Breast Cancer: Stage IV with poor prognostic indicators including but not limited to: a) >2 cytotoxic regimens for MBC; b) diagnosis of MBC less then or equal to 12 months since completion of adjuvant or neoadjuvant treatment; c) triple negative disease (ER/PR - and Her 2-);d) parenchymal brain mets and/or carcinomatous meningitis
    • Gastrointestinal (GI) Cancers: Unresectable stage III or IV
    • Genitourinary (GU) Cancers: Stage IV (for prostate cancer inclusion is limited to persons with hormone refractory prostate cancer)
    • Brain Cancer: Unresectable, Grade IV
    • Melanoma, Stage IV
    • Hematologic Malignancies -Leukemia (e.g. acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML), chronic lymphocytic leukemia (CLL) - advanced stage, treatment refractory, poor prognosis cell type or chromosomal abnormalities, "older age" -Lymphoma- Stage IV or treatment refractory Hodgkin's disease or non-Hodgkin's lymphoma -Multiple Myeloma - elevated β2-microglobulin, albumin <3.5, PCLI >1%, CRP >6µg/mL, elevated LDH, plasmablastic morphology, abnormal. chromosome 13.
  6. Completion of baseline interview

INCLUSION CRITERIA FOR PATIENTS FOR BIOMARKER SUB-STUDY:

1. Only patients with lung, breast, GI, GU cancer are eligible

INCLUSION CRITERIA FOR CAREGIVERS:

  1. Able to read and understand English
  2. Anyone identified by the patient as "a person who knows you well & is involved in your medical care".

PATIENT EXCLUSION CRITERIA:

  1. Dementia or significant confusion (Impaired cognitive status as indicated by a score of 3 or less on the Callahan six-item cognitive screening tool 18)
  2. Axis I psychiatric diagnosis of severe mental illness (DSM-IV) (e.g. schizophrenia, bipolar disorder, or active substance use disorder)
  3. Patients will not be excluded if they do not identify a caregiver
  4. Prior involvement with palliative care service within the last year
  5. Minimum predicted survival of less than 12 weeks (3 months)

PATIENT BIOMARKER SUBSTUDY EXCLUSION CRITERIA:

  1. Receiving chronic steroid hormones or unable to schedule specimen collection distant from chemotherapy from steroid pre-medications
  2. Unable to come to Norris Cotton Cancer Center (NCCC) for specimen collection times.

CAREGIVER EXCLUSION CRITERIA:

1. Unwilling to participate in study.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Terapia di supporto
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Early entry group
Early entry group will begin the intervention at time of diagnosis of advanced cancer
  1. Advanced Practice Palliative Care Nurse Interventionist instituting a phone-based: a) Charting Your Course (CYC)-Patient Curriculum (6-session manualized); b) Creativity Optimism Planning Expert information(COPE) Caregiver Curriculum (3 session manualized) and c) ongoing contact as determined by the Palliative Care Team assessment/plan; and
  2. Comprehensive Palliative Care Team Assessment & Management Plan.
Comparatore attivo: Later entry group
Later entry group will begin the intervention 12 weeks after enrollment in the study.
  1. Advanced Practice Palliative Care Nurse Interventionist instituting a phone-based: a) Charting Your Course (CYC)-Patient Curriculum (6-session manualized); b) Creativity Optimism Planning Expert Information (COPE) Caregiver Curriculum (3 session manualized) and c) ongoing contact as determined by the Palliative Care Team assessment/plan; and
  2. Comprehensive Palliative Care Team Assessment & Management Plan.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in patient's quality of living over time
Lasso di tempo: baseline, 6,12,18,24,36 and every 12 weeks until death or end of study

Quality of living assessments will include quality of life (QOL), mood, and symptom intensity measures using the following measures:

  • Functional Assessment of Chronic Illness Therapy-Palliative Care (FACIT-Pal):
  • Quality of Life at End of Life (QUAL-E).
  • Center for Epidemiological Study- Depression (CES-D).
baseline, 6,12,18,24,36 and every 12 weeks until death or end of study
Quality of end of life care
Lasso di tempo: chart review at time of death and caregiver proxy interview 2-3 months after patient death

End of life (EOL) Care Data Collection Form: This form is used to collect information about the quality of EOL care and circumstances surrounding the last 48 hours of life for patients who die in hospital, nursing home, or home.

Quality of Dying and Death Measure (QODD). The QODD is a structured interview conducted with a caregiver to measure the quality of a patient's last week of life. The interview assesses the caregiver's perception of patient symptoms, preferences, and satisfaction with care.

chart review at time of death and caregiver proxy interview 2-3 months after patient death
Estimate and compare the hazard ratios and median survival before and after 1 year from enrollment
Lasso di tempo: From enrollment until patient death or end of study
We hypothesize that Early entry patients will have longer overall survival at one year compared with Later entry patients.
From enrollment until patient death or end of study
Change in caregiver quality of life, burden and grief over time
Lasso di tempo: baseline, 6,12,18,24,36, and every 12 weeks until patient death or end of study

Caregiver burden and QOL will be measured using:

  • Quality of Life- Cancer- a self-report measure of QOL for caregivers of patients with cancer.
  • Montgomery Borgatta Caregiver Burden Scale -a self-report measure of caregiver burden.
  • Center for Epidemiological Study- Depression CESD is a measure of depressive symptoms.
  • Functional Assessment of Chronic Illness Therapy - Spiritual Module (FACIT-Sp) - a measure of spiritual well-being developed for persons with chronic illness.
  • Prigerson Inventory of Complicated Grief-Short form (ICG-SF) embedded in the Quality of Death and Dying (QODD).
baseline, 6,12,18,24,36, and every 12 weeks until patient death or end of study

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Mediating mechanisms and moderators of the concurrent palliative care intervention.
Lasso di tempo: baseline, 6,12,18,24,36 weeks and every 12 weeks until death or end of study

Mediating mechanisms measured will include patient activation, decision support, goal setting, problem solving, care coordination.

Moderators measures will include: decision control and treatment goals, self-efficacy, optimism, coping style, social support.

baseline, 6,12,18,24,36 weeks and every 12 weeks until death or end of study
Determine feasibility of enrolling less common solid tumors and hematologic malignancies.
Lasso di tempo: Estimated recruitment period of 2 years
ENABLE II recruited patients only with lung, breast, GI, and GU tumors. We will attempt to also recruit patients with less common "poor prognosis" solid tumors (e.g. brain) and hematologic malignancies and their caregivers for this concurrent oncology palliative care intervention.
Estimated recruitment period of 2 years
Explore patterns of stress (diurnal salivary and plasma cortisol) and immune biomarkers (lymphocyte subsets and cytokines)
Lasso di tempo: Baseline, 12, and 24 weeks

We will explore patterns of stress (diurnal salivary and plasma cortisol) and immune biomarkers (lymphocyte subsets and cytokines)at baseline, 12, and 24 weeks after intervention in a subset of 50 patients with breast, lung, GI, and GU cancer.

We hypothesize that stabilized or improved biomarkers of stress and immune function will be evident after Early and Later entry intervention participation.

Baseline, 12, and 24 weeks
Examine the relations among quality of life, mood, symptoms, survival, stress and immune biomarkers.
Lasso di tempo: Baseline, 12, and 24 weeks
We hypothesize that higher quality of life,mood, lower symptom intensity, and longer survival will be associated with stable or improved stress and immune biomarkers (e.g. normal plasma cortisol and diurnal salivary cortisol variability, lymphocyte subsets and cytokines
Baseline, 12, and 24 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Marie A. Bakitas, DNSc, APRN, Dartmouth-Hitchcock Medical Center
  • Direttore dello studio: Jennifer P. Frost, RN, MS, Dartmouth-Hitchcock Medical Center

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 ottobre 2010

Completamento primario (Effettivo)

1 settembre 2013

Completamento dello studio (Effettivo)

1 settembre 2013

Date di iscrizione allo studio

Primo inviato

15 novembre 2010

Primo inviato che soddisfa i criteri di controllo qualità

19 novembre 2010

Primo Inserito (Stima)

22 novembre 2010

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

3 gennaio 2014

Ultimo aggiornamento inviato che soddisfa i criteri QC

2 gennaio 2014

Ultimo verificato

1 ottobre 2013

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • NCCC-BAKI: D0946
  • R01NR011871-01 (Sovvenzione/contratto NIH degli Stati Uniti)

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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