Mobile Health Self-Management and Support System for Chronic and Complex Health Conditions
Primary Purpose
Spinal Cord Injuries, Cerebral Palsy, Spinal Dysraphism
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MHealth
Sponsored by
About this trial
This is an interventional supportive care trial for Spinal Cord Injuries focused on measuring Mobile health, Apps, Applications, Smart phone, mHealth, Chronic and Complex Conditions, Self-Management, Self-Care
Eligibility Criteria
Inclusion Criteria:
- 12 years or older.
- have a diagnosis of a chronic and complex condition such as Spina Bifida, Spinal Cord Injury, Cerebral Palsy and Traumatic Brain Injury, etc.
- live in a community setting (not within a residential facility that provides care to them).
- pass all the functional screening tests which include basic usage of a smart phone, and impairment severity assessments
Exclusion Criteria:
- Diagnosis of severe intellectual disability or severe and persistent psychiatric illness.
- Failing all the screening tests due to severe impairments that cannot be accommodated by the mHealth system (for patient participants)
Sites / Locations
- University of PittsburghRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
MHealth Group
Control
Arm Description
Participants randomized into this group will use the mHealth system throughout the study in conjunction with their standard of care
Participants randomized into this group will not use the mHealth system throughout the study, but will continue with their standard of care.
Outcomes
Primary Outcome Measures
Psychosocial Outcomes-Change of Self Management Skills Over Time as assessed by Self Management Questionnaire
Self management skill ratings measured at baseline, and approximately every three months for up to 12 months.
Psychosocial Outcomes-Change of Perceived Function and Satisfaction Over Time as assessed by Perceived Function and Satisfaction questionnaire.
Self ratings on perceived function and satisfaction questionnaire, assessed at baseline, and approximately every three months for up to 12 months.
Psychosocial Outcomes-Change of Quality of Life Over Time as assessed by Quality of Life questionnaire.
Quality of life ratings measured at baseline, and approximately every three months for up to 12 months.
Psychosocial Outcomes-Change of Function Ratings Over Time as assessed by Function or Physical Independence questionnaire.
Scale of Function measured at baseline, and approximately every three months for up to 12 months.
Psychosocial Outcomes- Change of Depressive Symptoms Over time as assessed by Depressive Symptoms questionnaire.
Questionnaire of Depressive symptoms administered at baseline, and approximately every three months for up to 12 months.
Medical Outcomes-Improvements in Preventable Conditions based on Medical Record Review
Medical record review of number of wounds, number of urinary tract infections and occurrences of sepsis.
Medical Outcomes-Improvements in Frequency of Health Care Utilization based on Medical Record Review and Questionnaire.
Medical Record Review and questionnaire on Number of hospitalizations, number of visits to emergency room and urgent care centers.
Medical Outcomes-Improvements in Length of Health Care Utilization based on Medical Record Review
Medical Record Review on Length of stay of hospitalizations.
Secondary Outcome Measures
Change of Participants' experience using the mHealth system over time as assessed by questionnaire
Questionnaire to assess participants subjective feelings about the use of the apps. This is for the MHealth group only.
Usage of the system as assessed by questionnaire and record review of the system usage (a built-in function in the system)
Questionnaire and review of usage record (a built-in function in the system) to measure the extent to which participants in the MHealth group consistently use the system to carry out their own self-management routines.
Cost of care
Estimated total cost of medical care.
Full Information
NCT ID
NCT02592291
First Posted
October 23, 2015
Last Updated
October 4, 2023
Sponsor
University of Pittsburgh
Collaborators
Department of Health and Human Services
1. Study Identification
Unique Protocol Identification Number
NCT02592291
Brief Title
Mobile Health Self-Management and Support System for Chronic and Complex Health Conditions
Official Title
Mobile Health Self-Management and Support System for Chronic and Complex Health Conditions (Component 3)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 2015 (undefined)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
September 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
Department of Health and Human Services
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will assess the benefits of using mobile health system designed for individuals with chronic and complex health conditions (such as those with Spinal Cord Injury,Cerebral Palsy, Spina Bifida, and Traumatic Brain Injury) to improve their wellness and self-management skills compared to those who receive standard of care only.
Detailed Description
Individuals with chronic and complex conditions such as those with spinal cord injury (SCI),Cerebral Palsy (CP), Spina Bifida (SB), and Traumatic Brain Injury (TBI), often require complex self-management routines to manage various needs such as bowel and bladder, skin integrity, and general health and wellness. Tasks such as self-catheterization, bowel regimens, skin checks, and routine administration of medications require consistent follow-through to prevent complications. Early detection and treatment of problems such as urinary tract infections (UTIs) or wounds, can prevent serious complications like osteomyelitis and sepsis which can result in hospitalization, death, and expensive medical care. The investigators have developed an innovative mobile health (mHealth) system aimed at improving self-management skills and preventing and detecting early signs of secondary medical complications. The system consist of a mobile health applications (apps), a clinician portal and a two-way secure communication system between the two. People with complex care regimens can use the apps to get reminders or cues to carry out their self care routines such as bowel/bladder routines, take medications, report success with their activities or new problems (e.g. new wound, UTI symptoms etc.), and track symptoms of depression. A clinician can use the portal to view the report and communicate with the users through a secure communication system that is embedded in the apps.
This study will assess the benefits of using the system in improving users' wellness and self-management skills compared to those who receive standard of care only.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injuries, Cerebral Palsy, Spinal Dysraphism, Brain Injuries, Spina Bifida, Traumatic Brain Injury
Keywords
Mobile health, Apps, Applications, Smart phone, mHealth, Chronic and Complex Conditions, Self-Management, Self-Care
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
160 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MHealth Group
Arm Type
Experimental
Arm Description
Participants randomized into this group will use the mHealth system throughout the study in conjunction with their standard of care
Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants randomized into this group will not use the mHealth system throughout the study, but will continue with their standard of care.
Intervention Type
Device
Intervention Name(s)
MHealth
Intervention Description
The Mhealth system consists of a suite of apps to support participants manage their self-care and the clinician portal. Participants will use the system for 1 year.
Primary Outcome Measure Information:
Title
Psychosocial Outcomes-Change of Self Management Skills Over Time as assessed by Self Management Questionnaire
Description
Self management skill ratings measured at baseline, and approximately every three months for up to 12 months.
Time Frame
At baseline and repeated on a schedule (approximately every three months) for up to 12 months
Title
Psychosocial Outcomes-Change of Perceived Function and Satisfaction Over Time as assessed by Perceived Function and Satisfaction questionnaire.
Description
Self ratings on perceived function and satisfaction questionnaire, assessed at baseline, and approximately every three months for up to 12 months.
Time Frame
At baseline and repeated on a schedule (approximately every three months) for up to 12 months
Title
Psychosocial Outcomes-Change of Quality of Life Over Time as assessed by Quality of Life questionnaire.
Description
Quality of life ratings measured at baseline, and approximately every three months for up to 12 months.
Time Frame
At baseline and repeated on a schedule (approximately every three months) for up to 12 months
Title
Psychosocial Outcomes-Change of Function Ratings Over Time as assessed by Function or Physical Independence questionnaire.
Description
Scale of Function measured at baseline, and approximately every three months for up to 12 months.
Time Frame
At baseline and repeated on a schedule (approximately every three months) for up to 12 months
Title
Psychosocial Outcomes- Change of Depressive Symptoms Over time as assessed by Depressive Symptoms questionnaire.
Description
Questionnaire of Depressive symptoms administered at baseline, and approximately every three months for up to 12 months.
Time Frame
At baseline and repeated on a schedule (approximately every three months) for up to 12 months
Title
Medical Outcomes-Improvements in Preventable Conditions based on Medical Record Review
Description
Medical record review of number of wounds, number of urinary tract infections and occurrences of sepsis.
Time Frame
Through study completion, an average of 1 year.
Title
Medical Outcomes-Improvements in Frequency of Health Care Utilization based on Medical Record Review and Questionnaire.
Description
Medical Record Review and questionnaire on Number of hospitalizations, number of visits to emergency room and urgent care centers.
Time Frame
Through study completion, an average of 1 year.
Title
Medical Outcomes-Improvements in Length of Health Care Utilization based on Medical Record Review
Description
Medical Record Review on Length of stay of hospitalizations.
Time Frame
Through study completion, an average of 1 year.
Secondary Outcome Measure Information:
Title
Change of Participants' experience using the mHealth system over time as assessed by questionnaire
Description
Questionnaire to assess participants subjective feelings about the use of the apps. This is for the MHealth group only.
Time Frame
At baseline and repeated on a schedule (approximately every three months) for up to 12 months)
Title
Usage of the system as assessed by questionnaire and record review of the system usage (a built-in function in the system)
Description
Questionnaire and review of usage record (a built-in function in the system) to measure the extent to which participants in the MHealth group consistently use the system to carry out their own self-management routines.
Time Frame
Through study completion, an average of 1 year.
Title
Cost of care
Description
Estimated total cost of medical care.
Time Frame
Through study completion, an average of 1 year.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
12 years or older.
have a diagnosis of a chronic and complex condition such as Spina Bifida, Spinal Cord Injury, Cerebral Palsy and Traumatic Brain Injury, etc.
live in a community setting (not within a residential facility that provides care to them).
pass all the functional screening tests which include basic usage of a smart phone, and impairment severity assessments
Exclusion Criteria:
Diagnosis of severe intellectual disability or severe and persistent psychiatric illness.
Failing all the screening tests due to severe impairments that cannot be accommodated by the mHealth system (for patient participants)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zara Ambadar, Ph.D.
Phone
412-608-6118
Email
ambadarz@upmc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andi Saptono, Ph.D.
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bambang Parmanto, Ph.D.
Organizational Affiliation
University of Pittsburgh
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Brad E. Dicianno, M.D.
Organizational Affiliation
University of Pittsburgh
Official's Role
Study Director
Facility Information:
Facility Name
University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15260
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zara Ambadar, Ph.D.
Phone
412-608-6118
Email
ambadarz@upmc.edu
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
31464189
Citation
Kryger MA, Crytzer TM, Fairman A, Quinby EJ, Karavolis M, Pramana G, Setiawan IMA, McKernan GP, Parmanto B, Dicianno BE. The Effect of the Interactive Mobile Health and Rehabilitation System on Health and Psychosocial Outcomes in Spinal Cord Injury: Randomized Controlled Trial. J Med Internet Res. 2019 Aug 28;21(8):e14305. doi: 10.2196/14305.
Results Reference
derived
Learn more about this trial
Mobile Health Self-Management and Support System for Chronic and Complex Health Conditions
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