search
Back to results

Mobile Intervention to Improve Adherence of Oral Anti-cancer Medications Among Acute Myeloid Leukemia Patients, the txt4AML Study

Primary Purpose

Acute Myeloid Leukemia

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Text Message-Based Navigation Intervention
Behavioral, Psychological or Informational Intervention
Survey Administration
Quality-of-Life Assessment
Sponsored by
Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Acute Myeloid Leukemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed with acute myeloid leukemia (AML)
  • Patients will be or is taking venetoclax (or any other oral anticancer medication) as part of their first line therapy
  • Has a phone with text capabilities
  • Among patients aged 18 and older we will enroll participants regardless of race or ethnicity

Exclusion Criteria:

  • Individuals who are terminally ill (defined as having less than 2 months to live)
  • Individuals for whom there is documentation of inability to provide consent in the medical record
  • Do not speak/read English
  • This study will exclude pediatric patients (defined as individuals under age 18 years)

Sites / Locations

  • Sidney Kimmel Cancer Center at Thomas Jefferson University
  • Thomas Jefferson University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Health services research (text messages, smart pill bottle)

Arm Description

Patients receive interactive text messages to help with adherence to medications and a smart pill bottle with medication reminders on study.

Outcomes

Primary Outcome Measures

Real-time oral anticancer medication (OAM) medication adherence
Will be measured daily by AdhereTech wireless smart pill bottles, which are Health Insurance Portability and Accountability Act (HIPAA)-compliant Food and Drug Administration (FDA) Class I medical devices that monitor electronic tracking of bottle and percent of pills detected inside the bottle. Will be summarized using proportions and 95% Clopper-Pearson exact confidence intervals.
Real-time oral anticancer medication (OAM) medication adherence
Will be measured daily by AdhereTech wireless smart pill bottles, which are Health Insurance Portability and Accountability Act (HIPAA)-compliant Food and Drug Administration (FDA) Class I medical devices that monitor electronic tracking of bottle and percent of pills detected inside the bottle. Will be summarized using proportions and 95% Clopper-Pearson exact confidence intervals.
Real-time oral anticancer medication (OAM) medication adherence
Will be measured daily by AdhereTech wireless smart pill bottles, which are Health Insurance Portability and Accountability Act (HIPAA)-compliant Food and Drug Administration (FDA) Class I medical devices that monitor electronic tracking of bottle and percent of pills detected inside the bottle. Will be summarized using proportions and 95% Clopper-Pearson exact confidence intervals.
MD Anderson Symptom Inventory for acute myeloid leukemia/myelodysplastic syndrome (MDASI)-(AML)/MDS survey response
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
MD Anderson Symptom Inventory for acute myeloid leukemia/myelodysplastic syndrome (MDASI)-(AML)/MDS survey response
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
MD Anderson Symptom Inventory for acute myeloid leukemia/myelodysplastic syndrome (MDASI)-(AML)/MDS survey response
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.

Secondary Outcome Measures

Complete remission (CR)
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence
Incomplete blood count recovery (Cri)
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Partial remissions (PR)
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Morphologic leukemia-free state (MLFS)
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.

Full Information

First Posted
October 18, 2022
Last Updated
July 31, 2023
Sponsor
Thomas Jefferson University
search

1. Study Identification

Unique Protocol Identification Number
NCT05595135
Brief Title
Mobile Intervention to Improve Adherence of Oral Anti-cancer Medications Among Acute Myeloid Leukemia Patients, the txt4AML Study
Official Title
txt4AML: An Innovative Mobile Intervention to Improve Oral Anti-Cancer Medications Among Acute Myeloid Leukemia Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Withdrawn
Why Stopped
staffing
Study Start Date
August 15, 2022 (Actual)
Primary Completion Date
May 5, 2023 (Actual)
Study Completion Date
May 5, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Thomas Jefferson University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This clinical trial studies how well a mobile intervention consisting of a text messaging program and an electronic "smart" pill bottle with medication reminders works to improve adherence to oral anti-cancer medications among patients with acute myeloid leukemia (AML). Medication adherence is how well patients take medications as prescribed by their doctors, and good medical adherence is when patients take medications correctly. Poor medication adherence has been shown to be a barrier to effective treatment. Collecting feedback on patient experiences using the mobile intervention may help doctors design new methods and material for providing educational information to AML patients who are taking oral anti-cancer medications.
Detailed Description
PRIMARY OBJECTIVE: I. To examine the feasibility, acceptability and preliminary efficacy of txt4AML in a pilot single arm study. SECONDARY OBJECTIVE: I. To explore the association between overall treatment responses and real-time oral anti-cancer medication (OAM) adherence. EXPLORATORY OBJECTIVE: I. To summarize and assess other patient-reported outcomes, collected either as patient chart review or through self-reported survey, as well as the patient post-intervention interviews. OUTLINE: Patients receive interactive text messages to help with adherence to medications and a smart pill bottle with medication reminders on study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Health services research (text messages, smart pill bottle)
Arm Type
Experimental
Arm Description
Patients receive interactive text messages to help with adherence to medications and a smart pill bottle with medication reminders on study.
Intervention Type
Other
Intervention Name(s)
Text Message-Based Navigation Intervention
Other Intervention Name(s)
Automated Text Message-Based Navigation, Text Message-Based Navigation
Intervention Description
Receive interactive text messaging.
Intervention Type
Other
Intervention Name(s)
Behavioral, Psychological or Informational Intervention
Intervention Description
Receive medication reminders via smart pill bottle
Intervention Type
Other
Intervention Name(s)
Survey Administration
Intervention Description
Ancillary studies
Intervention Type
Other
Intervention Name(s)
Quality-of-Life Assessment
Other Intervention Name(s)
Quality of Life Assessment
Intervention Description
Ancillary studies
Primary Outcome Measure Information:
Title
Real-time oral anticancer medication (OAM) medication adherence
Description
Will be measured daily by AdhereTech wireless smart pill bottles, which are Health Insurance Portability and Accountability Act (HIPAA)-compliant Food and Drug Administration (FDA) Class I medical devices that monitor electronic tracking of bottle and percent of pills detected inside the bottle. Will be summarized using proportions and 95% Clopper-Pearson exact confidence intervals.
Time Frame
At baseline
Title
Real-time oral anticancer medication (OAM) medication adherence
Description
Will be measured daily by AdhereTech wireless smart pill bottles, which are Health Insurance Portability and Accountability Act (HIPAA)-compliant Food and Drug Administration (FDA) Class I medical devices that monitor electronic tracking of bottle and percent of pills detected inside the bottle. Will be summarized using proportions and 95% Clopper-Pearson exact confidence intervals.
Time Frame
at 1 month
Title
Real-time oral anticancer medication (OAM) medication adherence
Description
Will be measured daily by AdhereTech wireless smart pill bottles, which are Health Insurance Portability and Accountability Act (HIPAA)-compliant Food and Drug Administration (FDA) Class I medical devices that monitor electronic tracking of bottle and percent of pills detected inside the bottle. Will be summarized using proportions and 95% Clopper-Pearson exact confidence intervals.
Time Frame
At 2 months
Title
MD Anderson Symptom Inventory for acute myeloid leukemia/myelodysplastic syndrome (MDASI)-(AML)/MDS survey response
Description
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Time Frame
At baseline
Title
MD Anderson Symptom Inventory for acute myeloid leukemia/myelodysplastic syndrome (MDASI)-(AML)/MDS survey response
Description
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Time Frame
At 1 month
Title
MD Anderson Symptom Inventory for acute myeloid leukemia/myelodysplastic syndrome (MDASI)-(AML)/MDS survey response
Description
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Time Frame
At 2 months
Secondary Outcome Measure Information:
Title
Complete remission (CR)
Description
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence
Time Frame
At baseline, 1, and 2 months
Title
Incomplete blood count recovery (Cri)
Description
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Time Frame
At baseline, 1, and 2 months
Title
Partial remissions (PR)
Description
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Time Frame
At baseline, 1, and 2 months
Title
Morphologic leukemia-free state (MLFS)
Description
Will be analyzed using univariable logistic regression models with the primary predictor of averaged daily real-time OAM medication adherence.
Time Frame
At baseline, 1, and 2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with acute myeloid leukemia (AML) Patients will be or is taking venetoclax (or any other oral anticancer medication) as part of their first line therapy Has a phone with text capabilities Among patients aged 18 and older we will enroll participants regardless of race or ethnicity Exclusion Criteria: Individuals who are terminally ill (defined as having less than 2 months to live) Individuals for whom there is documentation of inability to provide consent in the medical record Do not speak/read English This study will exclude pediatric patients (defined as individuals under age 18 years)
Facility Information:
Facility Name
Sidney Kimmel Cancer Center at Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Thomas Jefferson University Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Mobile Intervention to Improve Adherence of Oral Anti-cancer Medications Among Acute Myeloid Leukemia Patients, the txt4AML Study

We'll reach out to this number within 24 hrs