- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05070923
HealthyLifetime: Health Coaching for Older Adults
Healthy Lifetime (HL): an Internet-based Behavioral Health Coaching Protocol for Older Adults
Study Overview
Detailed Description
HL is an 8-week, personalized health coaching program that includes a comprehensive assessment made through a survey and a "virtual' home visit (via video), a goal-directed strengthening action plan developed by the participant with the guidance of the nurse, a tailored daily planning guide to enhance action steps and goal attainment, and six weekly 30 minute nurse coaching sessions with participants the Healthie application technology via their personal home computer, Tablet or Smartphone device. If a participant does not use a personal device or the device cannot support the Healthie platform, the HL program will provide a Tablet to them for their use during the program. All video sessions ( ie, home visit, strengthening plan, and weekly coaching sessions will use a two-way video but only the audio portions of the sessions will be recorded. The HL program, tailored to each participant's need for strong and resilient function, encompasses the following key elements:
Personal Health System Assessment (PHS Survey) - The foundational piece of HL is strengthening the participant's existing personal health system (PHS) - which we define as the network and interaction of an individual's strengths (such as beliefs, knowledge and skill for self-care and independence), social determinants of health, caregiver supports, and community resources, such as groceries, exercise, transportation, that the participant relies on to sustain health and function. The survey asks questions in the following domains: background information including income; social and spiritual network and support; personal health rating; use of healthcare services (emergency room visits, hospitalizations, primary care visits); lifestyle habits including use of tobacco, alcohol as well as diet, exercise, sleep and sexual behavior; health impact on activities, function, and symptoms; and self-efficacy in performing activities, in symptom management and in medication taking. The PHS Survey is completed by the participant through the web application and takes about 16 minutes to complete based on pilot data obtained in a sample of community living adults 50 years of age and older with one or more chronic conditions.
The PHS Survey results are reviewed by the UMSN Registered Nurse [either Advanced Practice Registered Nurse (APRN) or BSN- Prepared Registered Nurse (RN)] prior to the virtual home visit. During the virtual home visit, the nurse reviews the strengths of the PHS Survey, clarifies any information on the Medical History and conducts a home environment assessment completed by the participant under the guidance of the nurse. The nurse describes key results from the PHS Survey particularly focusing on their own words that describe their priority concerns and goals that they had expressed. The purpose of this is to maximize self-awareness and bring into focus the individual's own goals, strengths and areas for improvement forming the framework for beginning the PHS Plan process. The PHS Survey may reveal an individual's PHS network capacity (family, friends, community-organizations, church groups) to meet the person's need for additional in-home support for non-medical services such as housekeeping, bill paying, grocery shopping etc.
Personal Health System Strengthening Plan (PHS Plan) - The next step of the program includes creation of an individualized plan to strengthen capacity of the participant for self-care using the discussion of the PHS Survey and home assessments as a starting point for engaging the participant. The PHS Plan will be developed with the participant in a 45 - 60 minute video session the nurse. The PHS Plan assists the individual to set action steps to meet goals that reflect concerns about managing their medical regimen, medication taking, symptoms, daily living skills such as Activities of Daily Living (ADLs ) and Instrumental Activities of Daily Living (IADLs), and health behavior choices such as smoking, eating habits, activity etc. The nurse uses health coach motivational and nursing interviewing methods to support participant engagement, activation and self-efficacy in skills and decision-making. Goals and action steps progress throughout the 8-week program, with the guidance of the nurse, as the participant achieves success in reaching goals, making more independent choices, and gains self-care efficacy. By the conclusion of the HL program the participant is expected to have experienced the process of goal/action step/success so as to have sustaining capacity to continue the process without requiring the intensive support that HL provides.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Michigan
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Ann Arbor, Michigan, United States, 48109-5482
- University of Michigan School of Nursing
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 50 years of age or older who have one or more chronic medical conditions (e.g., high blood pressure, diabetes, arthritis, obesity, etc.) which require management in some way (regular doctor checks, medication, etc.);
- Whose health is medically stable; that is, not currently undergoing either significant physical and/or mental health changes and not undergoing any type of non-routine treatments/medical testing or have any surgeries scheduled in the next six months;
- Has not had an ER visit related to his/her chronic conditions in the prior one month (an ER visit related to a one-time, resolved issue such as a bee sting or to have stitches for a household injury will not be cause for exclusion);
- Is able to read, speak and hear English; may use adaptive devices such as hearing aid and glasses;
- Is able to recall personal information such as age, DOB, address, phone number, and health history questions without difficulty;
- Reports having an established internet connection that is regularly used for video content [such as with Netflix, Amazon Prime, YouTube]; and
- Is able to use their internet connection in a private space.
Exclusion Criteria:
- Are acutely ill or have unstable health problems requiring medical work-up or follow-up clinic visits for monitoring more than every 3 months;
- Have had an ER visit related to his/her chronic condition in the prior one month; (an ER visit related to a one-time, resolved issue such as a bee sting or to have stitches for a household injury will not be cause for exclusion);
- Are terminally ill;
- Have severe memory problems;
- Have severe hearing and/or visual deficits that are not functionally adapted with devices such as a hearing aid or eye glasses;
- Do not have an existing internet connection at the bandwidth needed to support the video platform [cannot access video streaming content]; and/or
- Is able to use internet only in a public space (unable to ensure privacy).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: HealthyLifetime Group
HL is an 8-week, personalized health coaching program that includes a comprehensive assessment made through a survey and a "virtual' home visit (via video), a goal-directed strengthening action plan developed by the participant with the guidance of the nurse, a tailored daily planning guide to enhance action steps and goal attainment, and six weekly 30 minute nurse coaching sessions with participants the Healthie application technology via their personal home computer, Tablet or Smartphone device.
If a participant does not use a personal device or the device cannot support the Healthie platform, the HL program will provide a Tablet to them for their use during the program.
All video sessions ( ie, home visit, strengthening plan, and weekly coaching sessions will use a two-way video but only the audio portions of the sessions will be recorded.
The HL program, tailored to each participant's need for strong and resilient function, encompasses the following key elements:
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HL augments existing case management services by focusing on building the participant's personal capacity for independence in self - care skills, health behavior change, and health decision making.
The HL program coordinates and interfaces with the enrollee's primary medical provider, case managers, and caregivers as necessary
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No Intervention: Usual Care Group
Participants randomized to the usual care group will be given information about when to expect reminders on the Healthie platform to complete future surveys at the end of week 8, and after three months that will be available on the Healthie Platform for them to fill out and save on the platform.
They will also be reminded how to contact the study coordinator if they should have questions.
Participants in this group will have the view to other functions on the platform turned off.
They will only be able to view documents as the reminders appear for them to complete.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Participant Self- rated health score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Participants perception of their health on a scale of 1= Excellent to 5 = Poor
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At 0, 8 and 12 weeks after study enrollment.
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Change in Self-efficacy in ability to continue essential life activities score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Confidence of the participant in doing certain activities on a scale of 1= Not at all confident to 10 = Totally Confident.
For the purposes of answering these questions, confidence is defined as the belief in the participant's chances of being able to do and/or complete an activity (e.g., hobbies and recreation, social visits, chores, errands, etc.) or task (e.g., hobbies and recreation, social visits, chores, errands, etc.) successfully however the participant defines it.
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At 0, 8 and 12 weeks after study enrollment.
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Change in Independent self care agency score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Confidence in doing certain activities, e.g., stick to behavior changes, meet goals, and improve health, on a scale of 1= Not at all confident to 10 = Totally Confident
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At 0, 8 and 12 weeks after study enrollment.
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Change in Health Habits score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Activities that participants engage in that affect health in a negative or positive way, e.g., smoking (yes or no), alcohol (number of drinks per week), exercise (0 = none to 4= more than 3 hours/week), food choices (seldom or never to 2 or more times a day)
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At 0, 8 and 12 weeks after study enrollment.
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Change in Goal attainment score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Health goals of participants (up to 3) and importance of goal (1= Not at all important now to 10 = highest importance now) and confidence in achieving goal (1= Not confident at all to 10 = Completely Confident)
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At 0, 8 and 12 weeks after study enrollment.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Sustained higher values of primary measures at 3 months
Time Frame: 12 weeks after study enrollment
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Are effects of program noted at 8 weeks still present at 12 weeks.
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12 weeks after study enrollment
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Change in Self-reported medical visits
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Number of unplanned medical visits with doctor or primary medical provider in past 3 months (0 = no visits to 8 = 7 or more), emergency room visits (0 = none to 3 = 2 or more), overnight stay in hospital (0 = none to 3 = 2 or more).
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At 0, 8 and 12 weeks after study enrollment.
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Perception of health now and in 3 years score
Time Frame: At 0, 8 and 12 week after study enrollments.
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Participant thinks health now is and in three years will be 1 = Excellent to 5 = Poor.
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At 0, 8 and 12 week after study enrollments.
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Change in Level of Symptomatology score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Frequency with which participants experience symptoms such as physical discomfort, pain, fatigue, etc. on a scale where 0 = Never to 5 = Always
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At 0, 8 and 12 weeks after study enrollment.
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Change in Confidence in ability to manage symptoms score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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How confident the participant is that they can keep health symptoms/problems from interfering with the things they want to do, e.g., fatigue, physical discomfort, emotional distress, etc. on a scale where 1 = Not at all Confident to 10 = Totally Confident
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At 0, 8 and 12 weeks after study enrollment.
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Change in Level of independence in activities score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Ability to do daily living activities such as shopping, cooking, managing medications, etc. on a scale where 1 = Not at all Confident to 10 = Totally Confident
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At 0, 8 and 12 weeks after study enrollment.
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Change in Medication taking self care efficacy score
Time Frame: At 0, 8 and 12 weeks after study enrollment.
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Confidence of participants (on a scale where 0 = Not at all Confident to 2 = very Confident) in taking their medications correctly under different conditions, e.g., if take several medication each day, are away from home, if cause side effects, etc.
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At 0, 8 and 12 weeks after study enrollment.
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Kathleen Potempa, PhD, University of Michigan
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- E20213681-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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