Myeloproliferative Neoplasms Clinical Trial

A Distress Reduction Intervention for Patients With BCR-ABL-Negative MPNs or CML on Tyrosine Kinase Inhibitors

Summary

This trial looks at how well a distress reduction intervention, called "Being Present", works to improve the quality of life of patients with BCR-ABL-negative myeloproliferative neoplasms (MPNs) or chronic phase chronic myeloid leukemia (CP-CML) who are taking tyrosine kinase inhibitors (TKIs) and their caregivers. Mindfulness meditation is the practice of repeatedly bringing attention back to the immediate experience and may help people cope with various types of illness, stress, and worry. This may help patients and caregivers to gradually learn to disconnect from reacting to and dwelling on the past and future and instead fully experiencing the present moment.

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Full Description

PRIMARY OBJECTIVES:

I. To tailor the Being Present intervention to BCR-ABL-negative MPN and CP-CML patients.

II. To determine the feasibility of an 8-week web-based mindfulness meditation program with live webinars among BCR-ABL-negative MPN patients and their caregivers, and CP-CML patients on tyrosine kinase inhibitors (TKIs), and CP-CML patients in treatment-free remission (TFR).

III. To determine the acceptability of an 8-week web-based mindfulness meditation program with live webinars among BCR-ABL-negative MPN patients and their caregivers, CP-CML patients on TKIs, CP-CML patients on TKIs, and CP-CML patients in TFR.

SECONDARY OBJECTIVE:

I. To evaluate the preliminary efficacy of the intervention.

EXPLORATORY OBJECTIVES:

I. To evaluate for differences in the feasibility and acceptability of an 8-week web-based mindfulness meditation program with live webinars:

Ia. Based on demographic or clinicopathologic factors. Ib. In patients versus caregivers.

II. To evaluate for differences in the preliminary efficacy an 8-week web-based mindfulness meditation program with live webinars:

IIa. Based on demographic or clinicopathologic factors. IIb. In BCR-ABL-negative patients versus caregivers. IIc. In BCR-ABL-negative patient-caregiver pairs versus unpaired patients. IId. Based on level of adherence to the practice instructions.

OUTLINE:

Patients and caregivers receive Being Present intervention consisting of online audio-based mindfulness meditation exercise over 15 minutes at least 5 times per week, daily meditation reminders, and online webinars over 30-60 minutes every week.

After completion of study, patients and caregivers are followed up at 8 weeks.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

PATIENT: Carry a diagnosis of BCR-ABL-negative MPN or CML
PATIENT: Have an estimated life expectancy of at least 6 months, assessed by principal investigator or treating investigator
PATIENT: Be able to speak and read English
PATIENT: Be able to navigate websites, fill out forms on the web, communicate by email, and have regular access to the internet (assessed by participant self-report)
PATIENT: Have daily access to a mobile phone capable of receiving text messages, as determined by a study investigator
PATIENT: Be able to provide informed consent
CAREGIVER: Be a spouse/partner, other family member, or a close friend of a BCR-ABL-negative patient who consented to participate in the Being Present-MPN study
CAREGIVER: Be able to speak and read English
CAREGIVER: Be able to navigate websites, fill out forms on the web, communicate by email, and have regular access to the internet (assessed by participant self-report)
CAREGIVER: Have access to a mobile phone capable of receiving text messages, as determined by a study investigator
CAREGIVER: Be able to provide informed consent

Exclusion Criteria:

PATIENT: Have had their BCR-ABL-negative MPN transform into acute leukemia
PATIENT: Have had their CP-CML transform into blast phase
PATIENT: Be post-allogeneic stem cell transplantation
PATIENT AND CAREGIVER: Have extensive hearing loss such that ability to participate in the study would be impaired

Study is for people with:

Myeloproliferative Neoplasms

Estimated Enrollment:

47

Study ID:

NCT04605211

Recruitment Status:

Completed

Sponsor:

University of California, San Francisco

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There is 1 Location for this study

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University of California San Francisco
San Francisco California, 94143, United States

How clear is this clinincal trial information?

Study is for people with:

Myeloproliferative Neoplasms

Estimated Enrollment:

47

Study ID:

NCT04605211

Recruitment Status:

Completed

Sponsor:


University of California, San Francisco

How clear is this clinincal trial information?

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