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mHealth Mindfulness With Patients With Serious Illness and Their Caregivers

Primary Purpose

Caregiver Stress Syndrome, Anxiety

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mindfulness Coach
Active Comparator
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Caregiver Stress Syndrome

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • adults 60+
  • Diagnosis of 2 or more serious illnesses (ESRD, Cancer, CHF, COPD, Liver Disease)
  • Hads-A > 8 for patient or caregiver
  • Blessed<6
  • fluent in English
  • vision and hearing does not interfere with mobile device use
  • caregivers who must be 21+
  • caregiver must identify as primary source of informal care for patient
  • Caregiver blessed <6
  • caregiver is fluent in English
  • Caregiver's vision and hearing does not interfere with mobile device use.

Exclusion Criteria:

  • experience with mindfulness therapy in last 2 years
  • not fluent in English
  • vision or hearing that impairs use of mobile device
  • cognitive impairment more than 6 on Blessed.

Sites / Locations

  • RWJ Barnabas Outpatient Geriatric ClinicsRecruiting
  • RWJB Outpatient GeriatricsRecruiting
  • Cancer Institute of New JerseyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

mindfulness coach

control - web MD

Arm Description

Mindfulness coach is an app that provides a training plan with 14 sequential levels, a "practice now" area with evidence-based mindfulness audio exercises, assessments using the Five-Factor Mindfulness Questionnaire Short Form (FFMQ-SF)90, and education about mindfulness an iOS- and Android-based app designed to deliver a mindfulness training course centered on Veteran's Affairs (VA) protocols. Developed by the VA's National Center for PTSD, the app provides an engaging introduction to MT, regardless of specific psychiatric illness or patient population. . To progress to the next level, the user must interact with every element. The training plan levels include psychoeducation and exercises (guided meditations and seated practices), which increase in duration as users progress. Levels 1,7 and 14 also include an assessment with the FFMQ-SF. The "practice now" area has guided meditations to practice new skills.

A a widely available health and wellness app that provides users with daily content on general health, WebMD, will serve as the attention control. Similar health-based apps have been used as controls in other mHealth psychotherapy intervention trials.100,101 The control group will be instructed to access the app 4x/week (same as intervention group) and will receive an orientation and 2 booster sessions as well. I considered other control group options including treatment as usual, but attention control was selected due to the variability of treatment as usual.

Outcomes

Primary Outcome Measures

Hospital Anxiety and Depression Scale - Anxiety Sub Scale
Anxiety scale with range from 0-21 with higher scores denoting highest anxiety
Hospital Anxiety and Depression Scale - Anxiety Sub Scale
Anxiety scale with range from 0-21 with higher scores denoting highest anxiety

Secondary Outcome Measures

Hospital Anxiety and Depression Scale - Depression Sub Scale
Depression scale with range from 0-21 with higher scores denoting highest depression
Hospital Anxiety and Depression Scale - Depression Sub Scale
Depression scale with range from 0-21 with higher scores denoting highest depression
Perceived stress scale
Scale with range from 0 - 40 with higher values indicating more perceived stress

Full Information

First Posted
September 7, 2021
Last Updated
March 27, 2023
Sponsor
Rutgers, The State University of New Jersey
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1. Study Identification

Unique Protocol Identification Number
NCT05040711
Brief Title
mHealth Mindfulness With Patients With Serious Illness and Their Caregivers
Official Title
Piloting an mHealth-delivered Mindfulness Therapy With Patients With Serious Illness and Their Caregivers to Alleviate Symptoms of Anxiety
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 26, 2022 (Actual)
Primary Completion Date
October 1, 2025 (Anticipated)
Study Completion Date
October 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey

4. Oversight

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

5. Study Description

Brief Summary
Older adults with serious illness and their caregivers have high rates of anxiety and limited access to effective, non-pharmacological treatments. A recent National Academy of Medicine report recommended increased emphasis on disseminating and implementing evidence-based psychotherapies in order to have maximal public health impact. Through this work, I will identify a sustainable and potentially scalable dyadic intervention and delivery model to manage symptoms of anxiety in older adults with serious illness and their caregivers in primary care.
Detailed Description
Research: Up to 70% of adults with serious illness have symptoms of anxiety. Undiagnosed and undertreated anxiety contributes to higher risk of pain, depression, fatigue, dyspnea, and polypharmacy. Patients with high symptom burden and anxiety heavily impact family caregivers, which nearly 8 million older adults in the U.S. rely on for assistance. Decades of research reveal the negative effects of caregiving on caregivers, (e.g., high levels of stress, depression, and anxiety). Furthermore, there is a mutuality of distress in the caregiver/patient dyad - when patients suffer psychologically, the caregiver suffers too. Unfortunately, older adults and their caregivers have limited access to mental health resources because of shortages of mental health providers as well as logistical issues including time constraints, transportation, and scheduling. The objective of this study is to evaluate the feasibility, acceptability, and preliminary efficacy of Mindfulness Coach, an mHealth Mindfulness Therapy intervention developed by the Veterans Affairs, to reduce anxiety in older adults with serious illness and their family caregivers. An efficacious and scalable behavioral intervention that mitigates symptoms of patient and caregiver anxiety has the potential to reduce distress and enhance coping in the patient-caregiver dyad without contributing to polypharmacy or burdensome appointments. Research is urgently needed to evaluate the feasibility, acceptability, and preliminary efficacy of dyadic mHealth mindfulness therapy in older adults with serious illness and their caregivers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Caregiver Stress Syndrome, Anxiety

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
162 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
mindfulness coach
Arm Type
Experimental
Arm Description
Mindfulness coach is an app that provides a training plan with 14 sequential levels, a "practice now" area with evidence-based mindfulness audio exercises, assessments using the Five-Factor Mindfulness Questionnaire Short Form (FFMQ-SF)90, and education about mindfulness an iOS- and Android-based app designed to deliver a mindfulness training course centered on Veteran's Affairs (VA) protocols. Developed by the VA's National Center for PTSD, the app provides an engaging introduction to MT, regardless of specific psychiatric illness or patient population. . To progress to the next level, the user must interact with every element. The training plan levels include psychoeducation and exercises (guided meditations and seated practices), which increase in duration as users progress. Levels 1,7 and 14 also include an assessment with the FFMQ-SF. The "practice now" area has guided meditations to practice new skills.
Arm Title
control - web MD
Arm Type
Active Comparator
Arm Description
A a widely available health and wellness app that provides users with daily content on general health, WebMD, will serve as the attention control. Similar health-based apps have been used as controls in other mHealth psychotherapy intervention trials.100,101 The control group will be instructed to access the app 4x/week (same as intervention group) and will receive an orientation and 2 booster sessions as well. I considered other control group options including treatment as usual, but attention control was selected due to the variability of treatment as usual.
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness Coach
Intervention Description
This study will use Mindfulness Coach, an iOS- and Android-based app designed to deliver a mindfulness training course centered on Veteran's Affairs (VA) protocols. Developed by the VA's National Center for PTSD, the app provides an engaging introduction to MT, regardless of specific psychiatric illness or patient population. The app provides a training plan with 14 sequential levels, a "practice now" area with evidence-based mindfulness audio exercises, assessments using the Five-Factor Mindfulness Questionnaire Short Form (FFMQ-SF)90, and education about mindfulness. To progress to the next level, the user must interact with every element. The training plan levels include psychoeducation and exercises (guided meditations and seated practices), which increase in duration as users progress. Levels 1,7 and 14 also include an assessment with the FFMQ-SF. The "practice now" area has guided meditations to practice new skills.
Intervention Type
Behavioral
Intervention Name(s)
Active Comparator
Other Intervention Name(s)
WebMD
Intervention Description
A a widely available health and wellness app that provides users with daily content on general health, WebMD, will serve as the attention control. Similar health-based apps have been used as controls in other mHealth psychotherapy intervention trials.100,101 The control group will be instructed to access the app 4x/week (same as intervention group) and will receive an orientation and 2 booster sessions as well. I considered other control group options including treatment as usual, but attention control was selected due to the variability of treatment as usual.
Primary Outcome Measure Information:
Title
Hospital Anxiety and Depression Scale - Anxiety Sub Scale
Description
Anxiety scale with range from 0-21 with higher scores denoting highest anxiety
Time Frame
6 months
Title
Hospital Anxiety and Depression Scale - Anxiety Sub Scale
Description
Anxiety scale with range from 0-21 with higher scores denoting highest anxiety
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Hospital Anxiety and Depression Scale - Depression Sub Scale
Description
Depression scale with range from 0-21 with higher scores denoting highest depression
Time Frame
6 months
Title
Hospital Anxiety and Depression Scale - Depression Sub Scale
Description
Depression scale with range from 0-21 with higher scores denoting highest depression
Time Frame
8 weeks
Title
Perceived stress scale
Description
Scale with range from 0 - 40 with higher values indicating more perceived stress
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: adults 60+ Diagnosis of or caregiver for individual with serious illnesses (e.g., ESRD, Cancer, CHF, COPD, Liver Disease) Hads-A > 8 for patient or caregiver Blessed<6 fluent in English vision and hearing does not interfere with mobile device use caregivers who must be 21+ caregiver must identify as primary source of informal care for patient Caregiver blessed <6 caregiver is fluent in English Caregiver's vision and hearing does not interfere with mobile device use. Exclusion Criteria: experience with mindfulness therapy in last 2 years not fluent in English vision or hearing that impairs use of mobile device cognitive impairment more than 6 on Blessed.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
ELISSA KOZLOV, PhD
Phone
9147153012
Email
elissa.kozlov@Rutgers.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Danielle Llaneza, MA
Email
dhl2132@tc.columbia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elissa Kozlov, PhD
Organizational Affiliation
Rutgers University
Official's Role
Principal Investigator
Facility Information:
Facility Name
RWJ Barnabas Outpatient Geriatric Clinics
City
Livingston
State/Province
New Jersey
ZIP/Postal Code
07039
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kim Wolf, BA
Facility Name
RWJB Outpatient Geriatrics
City
Monroe
State/Province
New Jersey
ZIP/Postal Code
08831
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kim Wolf, BA
Facility Name
Cancer Institute of New Jersey
City
New Brunswick
State/Province
New Jersey
ZIP/Postal Code
08901
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Daina Porter, BA

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

mHealth Mindfulness With Patients With Serious Illness and Their Caregivers

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