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TerminatedNCT03768401CHAMPsUpdated Apr 30, 2019

Accessible Mobile Health and Wellness

An interventional study of Education and Trial Exercise Modalities in Physical Disability and Neurologic Dysfunction, sponsored by Kristin Zhao, PhD. Terminated at 1 site in United States. Open to participants aged 6 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-04-30.

Sponsored by Kristin Zhao, PhD · Not applicable, Interventional, and Health services research

Why this study was terminated
Funding/grant expired.
Phase
Not applicable
Study type
Interventional
Enrollment
2
Allocation
Not applicable
Ages
6 Years to 65 Years
Sex
All
01

Study summary

Can community outreach education help develop self-sustaining wellness and exercise programs, and will associated wellness clinics help persons with a neurological physical disability achieve better well-being?

02

Conditions studied

  • Physical Disability
  • Neurologic Dysfunction
03

In context

Neurologic Manifestations

425 studies on the registry are indexed under Neurologic Manifestations; 82 are open to participants now.

This study's enrollment of 2 is below the median of 48 across 269 interventional studies indexed under Neurologic Manifestations.

Browse Neurologic Manifestations studies →

Lead sponsor

Kristin Zhao, PhD is the lead sponsor of 7 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • [for community participants/caregivers/family members] Ability to demonstrate clear communication and understanding of English.
  • [for participants with neurological physical conditions] Neurological physical conditions including cerebral palsy, spinal cord injury, stroke, multiple sclerosis, or similar diagnoses
  • [for educational seminars] > 6 years of age.
  • [for wellness/exercise clinic] 18 65 years of age
  • [for wellness/exercise clinic; participants with neurological physical conditions] Clearance by primary care or treating physician

Exclusion criteria

Exclusion Criteria:

  • [for participants with neurological physical conditions] Unstable fractures
  • [for participants with neurological physical conditions] Uncontrolled hypertension (combined systolic/diastolic > 140/90 mmHg)
  • [for participants with neurological physical conditions] Enrollment of individual deemed by study staff to be unsafe
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
2 participants (actual)

Study arms

  • Experimental
    Educational Seminars and Wellness Clinics

    I. Community outreach educational seminars about wellness and exercise while living with a neurological physical disability and measurement of the effects of these seminars for training individuals with neurological physical disabilities and their care givers (family, therapists, community personal trainers and community funders such as Lions or Rotary Clubs) about how to create a safe cost-effective exercise program . II. Creation and measurement of the effects of a wellness clinic for those with a neurological physical disability.

    Other: Education · Behavioral: Trial Exercise Modalities

Interventions

  • OtherEducation

    Seminars about wellness and exercise, and resulting therapeutic programs, while living with a neurological physical disability.

  • BehavioralTrial Exercise Modalities

    Wellness/exercise clinics located at Mayo Clinic, Rochester will be offered to persons with neurological physical disabilities on a regular basis, at least monthly, during the last half of the trial period.

06

What researchers measure

Primary outcomes

  1. Incidence of new self-sustaining wellness and exercise programs

    Incidence of new self-sustaining wellness and exercise programs, as determined by Follow-up Site Staff Survey

    Time frame: 3 months post end of wellness clinics

Secondary outcomes

  1. Efficacy of seminars for individuals with a neurological physical disability

    Efficacy of seminars, as determined by repeated t-tests based on the Exercise Self-Efficacy Survey (ESES), a 10-question survey with scores of 1 to 4 (with 4 being the best outcome), summed for a minimum score of 10, and a maximum score of 40.

    Time frame: 3 months post end of wellness clinics

  2. Efficacy of seminars for caregivers and clinic staff of patients with neurological physical disabilities

    Efficacy of seminars, as determined by repeated t-tests based on the Exercise Efficacy for Caregivers and Staff, a 10-question survey with scores of 1 to 4 (with 4 being the best outcome), summed for a minimum score of 10, and a maximum score of 40.

    Time frame: 3 months post end of wellness clinics

  3. Efficacy of wellness clinics

    Efficacy of wellness clinics, as determined by repeated t-tests

    Time frame: 3 months post end of wellness clinics

07

Study locations

1 site
  • Mayo Clinic in Rochester
    Rochester, Minnesota 55905, United States
08

References and documents

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 30, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03768401
Lead sponsor
Kristin Zhao, PhD
Collaborators
Southeastern Minnesota Center for Independent Living
Responsible party
Kristin Zhao, PhD (Principal Investigator, Mayo Clinic) — Sponsor-investigator
First posted
Dec 7, 2018
Start date
Aug 1, 2018
Primary completion
Dec 21, 2018
Completion
Dec 21, 2018
Last update
Apr 30, 2019

Study contacts

Kristin D Zhao
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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