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MGUS, SMM, and MM Patient Experience With Coronavirus 19 (COVID-19) Survey

H

HealthTree Foundation

Status

Unknown

Conditions

Multiple Myeloma
Monoclonal Gammopathy of Undetermined Significance
Smoldering Multiple Myeloma
Coronavirus

Treatments

Behavioral: Questionnaire

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04727294
MM/COVID-19 part II

Details and patient eligibility

About

The purpose of this study is to examine how patients with multiple myeloma (MM) have been impacted by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic.

The study will use a questionnaire to further understand how patients are being affected and gather information in order to track the long-term effects of the coronavirus.

The scope of the questionnaire will include, COVID-19 diagnosis and treatment, changes in myeloma treatment and care, clinical trial familiarity, health and fitness, and quality of life.

This questionnaire is a follow-on to the "MM and COVID-19" questionnaire.

Enrollment

1,500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Adult patients (greater than 18 years) diagnosed with MGUS, smoldering myeloma, and multiple myeloma.
  • Access to a computer or electronic device with internet access, or phone
  • Willing to create a patient profile on the HealthTree Cure Hub For Multiple Myeloma
  • Willing to give electronically-signed consent
  • Ability to read questions in English

Trial design

1,500 participants in 1 patient group

MGUS, SMM, MM Patients or their Caregivers
Description:
Eligible participants will be asked to create a free patient profile on the HealthTree Cure Hub (www.healthtree.org) or use their existing patient profile. The creation of a HealthTree Cure Hub patient profile will serve as a screen for eligibility. Patients will complete a one-time questionnaire found on the HealthTree Cure Hub. Telephone assistance can be provided as needed. The questionnaire will take 20-30 minutes to complete.
Treatment:
Behavioral: Questionnaire

Trial contacts and locations

1

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Central trial contact

Nathan Sweeney, PhD

Data sourced from clinicaltrials.gov

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