Moving Foward With Myeloma (MFM)

Part of paid clinical trials in Maywood, Illinois.

Sponsor
Medical College of Wisconsin
Study ID
NCT07236502
Status
Not Yet Recruiting

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Conditions

  • Multiple Myeloma (MM)

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Immediate intervention — BEHAVIORAL
    16-session intervention that facilitates changes in nutrition and physical activity behaviors to promote improvements in physical function, Patient Reported Outcomes, body composition and general health
  • Waitlist — OTHER
    Participants will be asked to maintain their behavior over the 16 week waitlist period and will receive weekly text message relating positive messages unrelated to lifestyle

Study Details

The purpose of this project is to evaluate the impact of a 16-week lifestyle program that promotes changes in eating and exercise patterns. The main questions the study will answer are: Do improvements in eating and exercise patterns lead to improved physical function, quality of life and blood biomarkers of biologial aging among individuals with multiple myeloma? Participants will complete study activities 3-4 times during the study. 1. In-person assessment to measure physical function, height/weight, body composition, and includes a blood draw 2. Surveys completed online or on paper at home

Key Dates

Start date
Jan 30, 2026
Status verified
Jan 2026
Primary completion
Dec 15, 2029
Completion
Feb 28, 2030

Study Design

Enrollment
184 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Immediate Intervention
    16-session intervention that facilitates changes in nutrition and physical activity behaviors to promote improvements in physical function, Patient Reported Outcomes, body composition and general health. The intervention targets plant-based eating, increasing physical activity and strength training.
  • Active Comparator: Waitlist control
    Participants will be asked to maintain their behavior over the 16 week waitlist period and will receive weekly text message relating positive messages unrelated to lifestyle.

Primary Outcome Measure

Examine the efficacy of the intervention in producing post-intervention changes in performance-based physical function [ Time Frame: Baseline, Week 16, Week 32, Week 48 ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Loyola University ChicagoMaywoodIllinois60153
Patricia Sheean, PhD
[email protected]
464-220-9216
Patricia Sheean, PhD (PRINCIPAL_INVESTIGATOR)
Medical College of WisconsinMilwaukeeWisconsin53226
Melinda Stolley, PhD
[email protected]
414-955-7533

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