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OpenTrials
Completed

NCT Number: NCT02128789

Bring Communities and Technology Together for Healthy Aging

Technology has been created to help older adults age well in their homes, but adoption and acceptance have been slow. The researchers are developing a low-cost web-based technology, called Elder Tree, for older adults and caregivers to address key challenges older adults face, such as loneliness and isolation, falls, loss of driving privileges, relapsing from proven falls prevention strategies, and unreliable home services. Elder Tree is being developed and tested with older adults and caregivers to identify, 1) usability issues such as font size, navigation and interface (audio, video,text) and 2) content and tailoring issues such as identifying local resources and events. This study will employ a randomized longitudinal design comparing a control group to an intervention group over a 12-month period. Investigators hypothesize that older adults using Elder Tree will experience greater independence and quality of life when compared to the control group. Investigators will use quantitative measures to determine how much our intervention improves: quality of life and health system use. These measures will help us to determine the cost effectiveness of Elder Tree. Investigators will recruit and test Elder Tree in 3 Regional Aging and Disability Resource Centers; one urban, one suburban and one rural setting, so to account for environmental and community differences. The older adult and their caregiver will be randomized to the same treatment group. Investigators will measure the effect over the 12 month intervention period and a 6 month follow-up period at 18 months.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of WI Madison

Madison, Wisconsin, 53705, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 65 years or older
  • In need of IADL support
  • 1 years history or risk of hospitalization or falls
  • Resident of the following counties Milwaukee, WI, Waukesha Wi or Richland County
  • Must be able to read English at a 6th grade level.

Exclusion criteria

  • Under 65 years of age
  • Unable to read English
  • Not a resident of the above listed counties.

Treatment and study plan

Elder Tree website

Other

Elder Tree is a private, secure information, support and communication website developed for this study.

Primary outcomes

  1. Number of older adult subjects with increased independence and quality of life from baseline to 18 months

    Time frame: Change in independence and quality of life will be assessed at 6, 12 , 18 months

    Compared to the control group elders using Elder Tree will experience greater independence and quality of life and will have fewer unscheduled clinical and emergency room visits and hospital and nursing home stays.

Secondary outcomes

  1. Number of caregiver subjects with improved satisfaction

    Time frame: Change in improved caregiver satisfaction will be assessed at 6, 12 , 18 months

    Compared to the control group, caregivers using Elder Tree will experience improved satisfaction, coping and appraisal.

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • Agency for Healthcare Research and Quality (AHRQ)
  • National Institutes of Health (NIH)

Registry information

Acronym: ElderTree

Important dates

Study start
2011
Primary completion
2016
Study completion
2016
First posted
May 1, 2014
Registry last updated
Oct 27, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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