Impact of a Health Technology Intervention on Patient Activation in Multiple Myeloma

Sponsor
All4Cure (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05673083
Collaborator
GlaxoSmithKline (Industry)
200
24

Study Details

Study Description

Brief Summary

The goal of this pilot study is to evaluate the impact of All4Cure enrollment on patients with relapsed multiple myeloma. The main question it aims to answer are:

• Does All4Cure effect patient activation as assessed by the PAM-13 survey?

Participants will be asked to:
  • fill out quarterly PAM-13 surveys through the All4Cure website to assess patient activation.

  • fill out monthly Patient Reported Outcome (PRO) surveys through the All4Cure website.

  • fill out a baseline and exit All4Cure surveys through the All4Cure website to assess patient perceptions of All4Cure at the beginning and the end of the study.

Detailed Description

The goal of this pilot study is to evaluate the impact of All4Cure enrollment on patients with relapsed multiple myeloma.

This study uses surveys to assess attitudes and perceptions of patients with myeloma at baseline and following their enrollment into All4Cure. The PAM-13 surveys will be administered at baseline and at 3-month intervals for a total of 5 surveys over 12 months. Patient attitudes and perceptions about the All4Cure platform will be assessed at baseline and at 12 months. Physicians caring for patients enrolled in this study will be surveyed twice -- at baseline and when all their patients have completed the study. Additionally, all patients will receive monthly surveys to assess symptoms associated with myeloma and its treatment using 36 survey items obtained from Patient Reported Outcomes (PRO)-Common Terminology Criteria for Adverse Events (CTCAE).

The study has the following objectives:

Primary objective To evaluate the impact of All4Cure enrollment on patients with relapsed multiple myeloma. The primary endpoint is the effect of All4Cure on patient activation, as assessed by the PAM-13 survey (change in results from baseline survey to the last completed survey).

Secondary objectives:

To evaluate the feasibility (i.e., ≥50% approach-to-enrollment rate of eligible participants and ≥70% completion of at least two PAM-13 surveys over a 12-month period) and acceptability (i.e., ≤20% withdrawing from the study and ≤20% withdrawing from All4Cure) of participation in All4Cure's digital platform for survivors with multiple myeloma.

To evaluate associations between participant activation levels (as assessed by PAM-13) and symptom burden, as measured by the Patient Reported Outcomes (PRO)-Common Terminology Criteria for Adverse Events (CTCAE).

To evaluate patient expectations and perceptions of the utility of All4Cure in their care and their association with PAM-13 results.

To evaluate associations between patient participation in the All4Cure platform (e.g. patient visits to the platform, patient posts on the platform, All4Cure posts on patient dashboards, and provision of MyelomaMap™ reports) and PAM-13 results.

To evaluate physician expectations and perceptions of the utility of All4Cure in their care of patients with relapsed multiple myeloma and their association with the PAM-13 results of their patients.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Impact of a Health Technology Intervention on Patient Activation in Multiple Myeloma
Anticipated Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
Feb 1, 2025
Anticipated Study Completion Date :
Feb 1, 2025

Outcome Measures

Primary Outcome Measures

  1. Patient Activation [24 months]

    Patient activation emphasizes patients' willingness and ability to take independent actions to manage their health and care. A widely used definition equates patient activation with understanding one's role in the care process and having the knowledge, skill, and confidence to manage one's health and health care. A growing body of evidence shows that patients who are more activated have better health outcomes and care experiences. This will be assessed through the PAM-13 survey which has a scale of 1-4, with 4 being the highest level of patient activation and associated with the best patient outcomes and 1 being the lowest level of patient activation.

Secondary Outcome Measures

  1. Evaluate associations between Patient Activation and symptom burden [24 months]

    Evaluate associations between participant activation levels (as assessed by PAM-13) and symptom burden, as measured by the Patient Reported Outcomes (PRO)-Common Terminology Criteria for Adverse Events (CTCAE).

  2. Evaluate the feasibility and acceptability of participation in All4Cure's digital platform for survivors with multiple myeloma [24 months]

    evaluate the feasibility (i.e., ≥50% approach-to-enrollment rate of eligible participants and ≥70% completion of at least two PAM-13 surveys over a 12-month period) and acceptability (i.e., ≤20% withdrawing from the study and ≤20% withdrawing from All4Cure) of participation in All4Cure's digital platform for survivors with multiple myeloma.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. have a diagnosis of multiple myeloma that has relapsed one or more times.

  2. are aged 18 years and older.

  3. can read and e-consent to participate in the study.

  4. can speak English.

  5. can complete surveys at pre-specified intervals.

  6. have access to a device that would allow for the completion of surveys (including at home, at work, at the oncologist's office or elsewhere).

  7. are cared for by a physician who is enrolled in All4Cure.

Exclusion Criteria:
  1. Patients will be excluded who are unable to engage with All4Cure or are already participants in All4Cure.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • All4Cure
  • GlaxoSmithKline

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
All4Cure
ClinicalTrials.gov Identifier:
NCT05673083
Other Study ID Numbers:
  • All4Cure02
First Posted:
Jan 6, 2023
Last Update Posted:
Jan 11, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by All4Cure
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2023