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Clinical Trials/NCT06458127
NCT06458127
Active, Not Recruiting
N/A

Tele-Palliative Care Intervention for Patients With Chronic Graft-Versus-Host Disease

Massachusetts General Hospital2 sites in 1 country10 target enrollmentSeptember 9, 2024

Overview

Phase
N/A
Intervention
Tele-palliative care visit
Conditions
Chronic Graft-versus-host Disease
Sponsor
Massachusetts General Hospital
Enrollment
10
Locations
2
Primary Endpoint
Feasibility of the tele-palliative care intervention as measured by the proportion of enrolled participants who complete at least two of the three intervention visits
Status
Active, Not Recruiting
Last Updated
26 days ago

Overview

Brief Summary

This research study is evaluating the feasibility and acceptability of implementing a telehealth palliative care intervention in patients with moderate to severe chronic graft-versus-host disease.

Detailed Description

Chronic graft-versus-host disease (cGVHD) is a major cause of morbidity among survivors of allogeneic hematopoietic cell transplantation (HCT) patients. Allogeneic HCT is a potentially curative procedure for a variety of hematologic malignancies and involves infusion of donor cells to establish marrow and immune function. Recent advances in risk determination, treatment (i.e., improved safety, use of a variety of donors), prevention of complications, and reduced-toxicity regimens have expanded the eligible patient population, and increased survival of patients who undergo HCT. However, development of cGVHD is a leading complication of allogenic HCT and impacts over 50% of survivors. It develops 3-18 months post-allogeneic HCT and is a main cause of post-HCT morbidity and mortality. cGVHD is a debilitating immunologic syndrome which attacks different organs in the body, resulting in a wide range of disruptive and unpredictable symptoms. Additionally, side effects of cGVHD include psychological distress with many patients reporting clinical levels of depression and anxiety. Further, patients with cGVHD are also at high risk for late effects, such as skeletal complications, secondary cancers, cardiovascular disease, and thromboembolic events. As a result of this diverse symptom burden, the side effects and psychological distress from illness, and uncertainty of the illness course, patients living with cGVHD experience diminished QOL. Patients with cGVHD struggle to manage their chronic condition, exacerbated with treatment related side effects of physical symptoms, functional limitations, psychological distress, and impaired QOL. Specialty palliative care clinicians have expertise in complex symptom management, facilitate coping with illness and improvement of QOL in cancer patients. Telehealth in various forms has been long studied as an approach to increase access to care, and a care model for management of chronic diseases. Expanding on prior experience with the specialty palliative care model for HCT patients, the investigators aim to develop a telehealth specialty PC model for patients with moderate to severe cGVHD. In this single-arm pilot study, the investigators will test the feasibility and acceptability of a once a month tele-palliative care appointment over the course of 3 months to address the symptom burden, psychological distress and disease uncertainty of cGVHD patients.

Registry
clinicaltrials.gov
Start Date
September 9, 2024
End Date
December 30, 2027
Last Updated
26 days ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

El-Jawahri, Areej,M.D.

Associate Professor of Medicine

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • 1\) Adult patients (\>18 years)
  • 2\) Have moderate to severe cGVHD based on their oncology clinician assessment as documented in the electronic health record.
  • 3\) Ability to comprehend and speak English, and to read and respond to questions in English
  • Please note that this is a proof-of-concept study, and we only include patients who comprehend, read, and respond to questions in English since the study instruments are all available in English. However, as we have done in prior studies, we will expand the population in a future efficacy trial.

Exclusion Criteria

  • 1\) Patients with acute or unstable psychiatric or cognitive conditions which the treating clinicians believe prohibits informed consent or compliance with study procedures
  • 2\) Patients who have already consulted or are currently consulting palliative care

Arms & Interventions

Tele-PC Intervention

Participants (individuals with moderate to severe chronic Graft-versus-Host Disease) will receive a monthly at home consultation with a specialty palliative care clinician via a video-conference tele-health visit.

Intervention: Tele-palliative care visit

Outcomes

Primary Outcomes

Feasibility of the tele-palliative care intervention as measured by the proportion of enrolled participants who complete at least two of the three intervention visits

Time Frame: Week 12

To calculate the feasibility of the intervention using the proportion of enrolled participants who complete at least two of the three intervention visits, with 95% confidence interval. The intervention will be deemed feasible if at least 70% of participants attend at least two of the three intervention visits.

Feasibility of the tele-palliative care intervention as measured by the proportion of eligible patients who are approached and agree to participate

Time Frame: Week 12

To calculate the feasibility of the intervention using the proportion of eligible patients who are approached and agree to participate, with 95% confidence interval. The intervention will be deemed feasible if at least 60% of patients with moderate to severe cGVHD agree to participate in the study.

Secondary Outcomes

  • Acceptability of the tele-palliative care intervention as measured by the Client Satisfaction Questionnaire(Week 12)

Study Sites (2)

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