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PatIent exPeRiences and prEFerence of trEatment foR Multiple Myeloma

PatIent exPeRiences and prEFerence of trEatment foR Multiple Myeloma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06322927
Acronym
iPREFER
Enrollment
9
Registered
2024-03-21
Start date
2024-04-05
Completion date
2024-09-30
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Myeloma

Keywords

Patient Experience, Treatment Preference, Qualitative Study, Patient Interviews

Brief summary

This is a qualitative (interview) study to explore the experiences of people receiving treatment for MM and to understand what matters most to participants when making treatment decisions.

Detailed description

People can receive many lines of treatment for multiple myeloma. The investigators would like to understand more about the experiences of people being treated for multiple myeloma including what matters most to participants when considering treatment options, how participants experiences have differed with different treatments and if participants have any treatment preferences. Patients at The Christie who have received five or more lines of treatment for Multiple Myeloma will be eligible to take part in this study. Participants will be asked to take part in an interview which should take approximately 30 minutes to an hour. During the interview, participants will be asked questions regarding their experiences and preference for treatment. Interviews will be conducted either in person or over the phone depending on patient preference. The interviews will be recorded by the research team using a Dictaphone and transcribed by an external transcription service called 1st Class Secretarial. The transcripts of all participant interviews will be reviewed by members of the research team and experiences will be identified and described.

Interventions

Participants will be asked to take part in a 30-60 minute interview to understand their treatment experiences and preferences.

Sponsors

The Christie NHS Foundation Trust
Lead SponsorOTHER
CellCentric Ltd.
CollaboratorINDUSTRY

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Participants with confirmed MM (per standard disease specific diagnostic criteria) 2. Participants must have received ≥ 5 lines of treatment for MM and fit into one of the below treatment categories: 1. Subset 1- Participants must have received an oral anti-cancer therapy and a bi-specific antibody treatment. 2. Subset 2- Participants must have received an oral anti-cancer therapy and if they have not had a bi-specific antibody treatment, they must have received at least one IV therapy. 3. Aged 18 years of age or over 4. Able to provide informed consent 5. Able to communicate in English

Exclusion criteria

1. Aged under 18 2. Unable to understand and communicate in the English language 3. Unable to provide written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Patient Experience and Preference30-60 minutesThe interview will explore the experiences of people receiving treatment for multiple myeloma and understand what matters most to them when making treatment decisions.

Secondary

MeasureTime frameDescription
Treatment and Preference Differences30-60 minutesThe interview will explore how experiences have differed across different lines of treatment and determine if people with multiple myeloma have any preferences for particular treatments.

Countries

United Kingdom

Contacts

PRINCIPAL_INVESTIGATORSally Taylor, PhD

The Christie NHS Foundation Trust

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026