The Myeloma Pack: A Multi-Modality Educational Intervention Strategy to Engage Patients With Multiple Myeloma

Who is this study for? Patients with Multiple Myeloma
What treatments are being studied? MPI Educational Program
Status: Completed
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Multiple Myeloma (MM) patients are prone to poor quality of life (QoL) as a result of the anxiety and depression they suffer due to a poor understanding of their disease. Improving patient understanding of their illness and addressing issues that induce distress impacts QoL. This prospective, interventional study is designed to see if a structured psycho-educational program called the myeloma pack intervention (MPI), implemented in parallel with standard cancer treatment, can improve QoL for patients with MM.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Of age ≥18 years or older.

• Having a diagnosis of MM; newly diagnosed or relapsed/refractory disease

• Undergoing systemic treatment through the UAB MM Clinic Pathway

• Able to provide informed consent to be included in the intervention

• MM patients in a prior/concurrent (non-pyscho/educational intervention), MM study will be eligible to participate

• Have either SMS texting or email access to receive encouragement messages

Locations
United States
Alabama
University of Alabama at Birmingham
Birmingham
Time Frame
Start Date: 2017-11-27
Completion Date: 2024-11-22
Participants
Target number of participants: 85
Treatments
Experimental: ARM A EARLY INTERVENTION GROUP
In Arm A, the intervention group, the participants will start on the program immediately. The participants will receive MPI educational program, implemented in parallel with standard of care treatment. The MPI is implemented at the time of enrollment x 12 weeks
Experimental: ARM B DELAYED INTERVENTION GROUP
Arm B, is a wait-list control group that will serve as the control. The wait-list control group will be observed for an initial 12 week period while receiving usual care and then have the educational intervention implemented from week 12-24 in parallel with standard of care
Related Therapeutic Areas
Sponsors
Leads: University of Alabama at Birmingham

This content was sourced from clinicaltrials.gov