CClinicalTrials.gg
TerminatedNCT05276622PaCE-MMUpdated Dec 12, 2024

Patient and Care Partner Experiences Living With Multiple Myeloma (PaCE-MM)

An observational study in Multiple Myeloma, sponsored by UNC Lineberger Comprehensive Cancer Center. Terminated at 1 site in United States. Open to participants aged 55 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-12-12.

Sponsored by UNC Lineberger Comprehensive Cancer Center · Observational

Why this study was terminated
Investigator left the institution.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
64
Ages
55 Years and older
Sex
All
01

Study summary

This research study is explore the impact over time of multiple myeloma and its associated treatments on the physical and cognitive function and quality of life of patients and their care partners and how these impacts affect the overall illness experience.

Read the detailed description

This study aims to identify the factors, for example, age, race, sex, education, household income, clinical or other geriatric conditions such as depression, anxiety, or lack of social support that can predict those most likely to experience changes in physical and cognitive function and quality of life. Furthermore, patients and care partners experienced challenges, because of multiple myeloma and its associated treatments, will be studied using semi-structured interviews.

Patients will complete baseline geriatric assessments and a 30-45-minute cognitive test, and both will be reassessed in 3 months intervals. The geriatric assessment is primarily patient-reported surveys and involves a multi-domain evaluation of a patient's functional status (i.e., their ability to live independently at home and in the community), co-morbid medical conditions, cognition, psychological status, social functioning and support, medications, and nutritional status. Care Partners will be asked to complete baseline surveys that will also assess their well-being and ability to function at home.

To provide a more comprehensive understanding of the myeloma-related experiences a subset of patients and their care partners will be asked to participate in a baseline interview repeated over time to understand how the disease and its treatments shape the experiences.

Duration of Subject Participation: 6 months

02

Conditions studied

  • Multiple Myeloma

Keywords

  • Newly diagnosed multiple myeloma
  • Physical Function
  • Cognitive Function
  • Quality of Life
  • Geriatric Assessments
  • Care partners
03

In context

Multiple Myeloma

3,632 studies on the registry are indexed under Multiple Myeloma; 745 are open to participants now.

This study's enrollment of 64 is below the median of 140 across 468 observational studies indexed under Multiple Myeloma.

Browse Multiple Myeloma studies →

Lead sponsor

UNC Lineberger Comprehensive Cancer Center is the lead sponsor of 414 studies on the registry; 95 are open to participants now.

Of its 32 completed or terminated interventional studies of FDA-regulated products, 25 (78%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
55 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study has two different population groups: A. Forty subjects with newly diagnosed multiple myeloma did not receive treatment yet., B. Thirty care partners of the subjects with newly diagnosed multiple myeloma did not receive treatment yet.

Inclusion criteria

Patients must meet the following inclusion criteria to participate in this study:

  1. Aged ≥55
  2. New myeloma diagnosis as defined by the International Myeloma Working Group, does not have another non-myeloma plasma cell disorder such as POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, skin changes) or amyloidosis.
  3. Starting systemic treatment.
  4. Able to understand and speak in English.
  5. Able to provide informed consent to participate.

Care Partners must meet the following inclusion criteria to participate in this study

  1. Aged ≥18.
  2. Able to understand and speak in English.
  3. Able to provide informed consent to participate.
  4. Be a care partner for a patient with multiple myeloma and is also enrolled in the assessment portion of this study.
  5. Willing and able to participate in semi-structured interviews.

Exclusion criteria

Exclusion Criteria:

  1. All participants meeting any of the following exclusion criteria at enrollment will be excluded from the study: Inability to read and speak English.
  2. Dementia altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
64 participants (actual)
Patient registry
No

Groups and cohorts

  • Subjects with newly diagnosed multiple myeloma

    Forty subjects with newly diagnosed multiple myeloma.

    Other: Comprehensive Geriatric Assessment

  • Care partners of the subjects with newly diagnosed multiple myeloma

    Thirty care partners of the subjects with newly diagnosed multiple myeloma.

    Other: Qualitative patient-care partner interviews · Other: Surveys on well-being and function

Interventions

  • OtherComprehensive Geriatric Assessment

    A modified Cancer and Aging Research Group (CARG) Geriatric Assessment that includes validated measures of 7 geriatric domains: functional status, comorbidity, cognition, psychological state, social activity, and support, nutritional status, and medications will be performed at baseline (pre-treatment), every 3 months for a total of 3 assessments. The modified comprehensive Geriatric Assessment includes patient-reported surveys and research staff assessments. Cognitive Testing: The National Institutes of Health Toolbox Cognition Battery (objective) and PROMIS Short Form v2.0 - Cognitive function 8a (subjective)

  • OtherQualitative patient-care partner interviews

    Semi-structured Interviews: Baseline and again at 3 months.

  • OtherSurveys on well-being and function

    Care partner's Surveys on well-being and function: Baseline and again at 3 months

06

What researchers measure

Primary outcomes

  1. Trajectories of cognitive functions NIHTB-CB

    Standardized National Institutes of Health Toolbox Cognition Battery (objective) (NIHTB-CB) will be used for the measure of cognitive function. The NIHTB-CB contains 7 computer-based instruments assessing 5 cognitive sub-domains: Language, Executive Function, Episodic Memory, Processing Speed, and Working Memory. The Composite Score is calculated using all subsets. Higher score =better level of cognitive functions.

    Time frame: Up to 6 months

  2. Trajectories of cognitive functions PROMIS

    Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form v2.0 - Cognitive function 8a (subjective) scores will be combined for an overall measure of cognitive function. PROMIS Short Form v2.0- Cognitive function 8a is a participant reported measure of cognitive function. There are 8 questions, with a possible raw score of 8 to 40, then converted into a T-score for each participant. T-scores lower below 50 indicate a lower than average cognitive performance.

    Time frame: Up to 6 months

  3. Trajectories of HRQoL cognitive functions

    The European Organization for Research and Treatment of Cancer Quality-of-Life questionnaire (EORTC QLQ-C30) will be used to measure the changes in quality of life. EORTC QLQ-C30 is a 30-item questionnaire to assess the overall quality of life in cancer patients. EORTC QLQ-C30 includes functional scales (physical, role, cognitive, emotional, and social), global health status, symptom scales (fatigue, pain, nausea/vomiting), and other (dyspnea, appetite loss, insomnia, constipation/diarrhea, and financial difficulties). Most questions used 4-point scale (1 'Not at All' to 4 'Very Much'); 2 questions used 7-point scale (1 'Very Poor' to 7 'Excellent'). Scores are averaged, and transformed to 0-100 scale; higher score=better level of physical functioning.

    Time frame: Up to 6 months

  4. Trajectories of physical function measured by ADLs

    The physical function will be measured using participant-reported activities of daily living (ADLs) as bath, dress, toilet, transfer bed to chair, maintain continence and feed. The score ranges from 0-6 with an increasing score indicating loss of independence/function.

    Time frame: Up to 6 months

  5. Trajectories of physical function measured by IADLS

    The physical function will be measured using Older Americans Resources and Services (OARS) instrumental activities of daily living (IADLS). Participants are asked to self-report their ability to engage in the following activities of daily living: bathe, dress, feed, toilet, maintain continence, transfer from bed to chair, use the telephone, shop, prepare food, housekeeping, laundry, take medications, manage finances, use transportation. The score ranges from 0-8 with an increasing score indicating loss of independence/function.

    Time frame: Up to 6 months

  6. Trajectories of physical function measured by Gait speed

    The physical function will be measured using gait speed. Gait speed is measured by having participants walk at their normal pace at a distance of 4 meters. The slower the gait speed the more likely an individual is likely to be impaired functionally.

    Time frame: Up to 6 months

Secondary outcomes

  1. Predictors of changes in cognitive function

    Multivariable regression modelling will be used to examine whether or not the following participant-reported socio-demographics factors (age, race, sex, education, income, community social vulnerability) and geriatric conditions (medical comorbidities, depression, anxiety, lack of social support) can predict those most likely to experience changes in cognitive function over a 6- month period.

    Time frame: Up to 6 months

  2. Predictors of changes in physical function

    Multivariable regression modelling will be used to examine whether or not the following participant-reported socio-demographics factors (age, race, sex, education, income, community social vulnerability) and geriatric conditions (medical comorbidities, depression, anxiety, lack of social support) can predict those most likely to experience changes in physical function (ADLS, IADLS, gait speed) over a 6-month period.

    Time frame: Up to 6 months

  3. Predictors of changes in quality of life

    Multivariable regression modeling will be used to examine whether or not the following participant-reported socio-demographics factors (age, race, sex, education, income, community social vulnerability) and geriatric conditions (medical comorbidities, depression, anxiety, lack of social support) can predict those most likely to experience changes in quality of life level based on the European Organization for Research and Treatment of Cancer Quality-of-Life questionnaire (EORTC QLQ-C30) scores, over 6- month period. Higher score=better level of physical functioning.

    Time frame: Up to 6 months

  4. Gain a complete understanding of the challenges patients and care partners living with multiple myeloma face

    Multiple myeloma and its associated treatments shape functional capacity, quality of life, and the overall illness experience in adults with multiple myeloma and their care partners will be evaluated using semi-structured interviews. Furthermore, changes between baseline, and at 3 months after treatment starts will be compared.

    Time frame: Up to 6 months

07

Study locations

1 site
  • Lineberger Comprehensive Cancer Center
    Chapel Hill, North Carolina 27514, United States
08

References and documents

Individual participant data

Plan to share: No — Deidentified individual data that supports the results will be shared beginning 9 to 36 months following publication provided the investigator who proposes to use the data has approval from an Institutional Review Board (IRB), Independent Ethics Committee (IEC), or Research Ethics Board (REB), as applicable, and executes a data use/sharing agreement with UNC.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05276622
Lead sponsor
UNC Lineberger Comprehensive Cancer Center
Collaborators
National Institute on Aging (NIA)
Responsible party
Sponsor
First posted
Mar 11, 2022
Start date
Feb 8, 2022
Primary completion
Oct 3, 2023
Completion
Oct 3, 2023
Last update
Dec 12, 2024

Study contacts

Shakira Grant, MBBS
principal investigator · Lineberger CCC, Center for Aging and Health, The University of North Carolina Chapel Hill

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion