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An Accessible and Inclusive Artificial Intelligence Assisted Chronic Disease Self-Management Telehealth Platform

The University of Alabama at Birmingham logo

The University of Alabama at Birmingham

Status

Enrolling

Conditions

Chronic Condition
Chronic Conditions, Multiple
Disability Physical

Treatments

Behavioral: Scheduled Coaching Calls + Independent Rewards
Behavioral: No Scheduled Coaching Calls + Gamified Rewards
Behavioral: Scheduled Coaching + Gamified Rewards
Behavioral: No Scheduled Coaching Calls + Independent rewards

Study type

Interventional

Funder types

Other

Identifiers

NCT05481593
IRB-300009485

Details and patient eligibility

About

The purpose of this study to pilot test an accessible and inclusive artificial intelligence (AI)-assisted, individualized, family-focused lifestyle modification intervention (AI4CHRON) for health-related quality of life for adults with impaired mobility and chronic medical conditions.

Full description

The AI4CHRON study will use a four-arm randomized control trial design. Eligible and consented participants will be assigned to one of four groups: 1) Scheduled coaching calls with gamified rewards, 2) Scheduled coaching calls with rewards independent of gamification, 3) No scheduled coaching calls with gamified rewards, and 4) No scheduled coaching calls with rewards independent of gamification. The active intervention period will be six months.

Enrollment

212 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years or older
  • Diagnosis of heart disease, chronic lung disease, or Type 2 diabetes
  • Living with a permanent physical disability (i.e., spina bifida, multiple sclerosis, stroke,)
  • Have the ability to converse in and read English
  • Availability of a smartphone or computer

Exclusion criteria

  • Current enrollment in any structured intervention
  • Severe cognitive impairment
  • Severe untreated depression in the past 6 months
  • Major cardiac event in the past 12 months
  • Uncontrolled blood pressure
  • Resting tachycardia
  • Renal failure
  • Severe peripheral neuropathy
  • Active treatment for cancer in the past 12 months
  • Having both visual and hearing impairments (either of them is fine)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

212 participants in 4 patient groups

Scheduled Coaching Calls & Gamified Rewards
Experimental group
Treatment:
Behavioral: Scheduled Coaching + Gamified Rewards
No Scheduled Coaching Call & Gamified Rewards
Experimental group
Treatment:
Behavioral: No Scheduled Coaching Calls + Gamified Rewards
Scheduled Coaching Calls & Independent rewards (No Gamification)
Experimental group
Treatment:
Behavioral: Scheduled Coaching Calls + Independent Rewards
No Scheduled Coaching Calls & Independent Rewards (No Gamification)
Experimental group
Treatment:
Behavioral: No Scheduled Coaching Calls + Independent rewards

Trial contacts and locations

1

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Central trial contact

Eric J Evans, PhD; Mohanraj Thirumalai, PhD

Data sourced from clinicaltrials.gov

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