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Personal Activity Intelligence (PAI) Pilot

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Ohio University

Status

Completed

Conditions

Hypertension
Diabetes
Dyslipidemias
Overweight and Obesity
Cardiovascular Diseases

Treatments

Behavioral: PAI

Study type

Interventional

Funder types

Other

Identifiers

NCT03740074
18-X-263

Details and patient eligibility

About

Pilot study to evaluate the use of the Personal Activity Intelligence (PAI) score in a clinical setting.

Full description

This is a pilot project to evaluate the feasibility of a larger study to evaluate the effectiveness of Personal Activity Intelligence (PAI) score in patients with chronic disease, as an adjunct to lifestyle medical therapy.

The PAI score is a proprietary formula developed by PAI Health (PH) to aid physical fitness. A PAI score calculation uses biometrics obtained via a device that measures heart rate and steps. For this study, Mio Slice, a commercial wrist worn device will be utilized to obtain data which will be linked to a smart phone. Data from the smart phone app will be accessed by PAI Health. Feedback information will be given to the participants to encourage increased physical activity.

The short-term aim of this study is to evaluate the logistics of utilizing PAI in the patient setting.

The data obtained from this study will be utilized to devise a larger study to evaluate the utility of PAI in patients with chronic disease who are receiving lifestyle medical therapy.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients who are seen by the PI in his lifestyle medicine practice at Muntean Health Care.
  • Participants must own a smart phone and feel comfortable managing apps on their smart phone.
  • Participants must be willing and able to register online with PAI Health (PH)
  • Participants must be willing to wear a wrist device around the clock, except when charging or bathing for 12 weeks.
  • Participants must have at least one of the following diagnoses:
  • overweight / obesity
  • diabetes or prediabetes
  • hypertension or pre-hypertension
  • abnormal lipids
  • cardiovascular disease

Exclusion criteria

  • Patients with angina or poor exercise tolerance, based on the evaluation by the PI, will be excluded from the study.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

PAI
Experimental group
Description:
Participants will utilize a MIO Slice wearable device to generate a PAI score, which will be utilized to provide feedback and incentive for physical activity.
Treatment:
Behavioral: PAI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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