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N/A N=344 Randomized Double-blind Supportive Care

Multiple Chronic Conditions for Older Adults

Chronic Disease

Enrolled (actual)
344
Serious AEs
0.0%
Results posted
Sep 2022
Primary outcome: Primary: PROMIS Global Health Measure Score — 46.27; 46.21; 44.92; 46.38 T-score

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Treatment as usual (TAU) + Internet (Other); TAU + ElderTree (Behavioral)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
University of Wisconsin, Madison
Primary completion
Jun 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
PROMIS Global Health Measure Score
46.27; 46.21; 44.92; 46.38; 42.40; 42.35
PRIMARY
Psychological Flourishing Scale
31.55; 31.12; 31.50; 31.48
PRIMARY
UCLA Loneliness Scale
16.02; 17.12; 16.05; 16.75
SECONDARY
Unhealthy Laboratory Scores
0.64; 0.64
SECONDARY
Falls
0.36; 0.36; 0.36; 0.72
SECONDARY
Symptom Distress
21.10; 20.58; 18.86; 18.58
SECONDARY
Medication Adherence
13.14; 13.07; 12.70; 12.56
SECONDARY
Crisis Health Care Visits
0.42; 0.45; 0.86; 0.76
SECONDARY
Long-term Care
0.01; 0.25; 0.79; 0.29
SECONDARY
Falls Requiring Medical Attention
0.23; 0.18; 0.33; 0.16

Summary

Multiple chronic conditions are common and expensive among patients aged ≥65 and are associated with lower quality of life, poorer response to treatment, worse medical and psychiatric outcomes, higher mortality, and higher costs of care. The primary purpose of this study is to conduct a randomized clinical trial (RCT) to examine the effects of ElderTree --a web-based intervention--on health outcomes and healthcare use among older adults with several chronic health conditions, such as diabetes, high blood pressure, high cholesterol, COPD, BMI over 30, congestive heart failure, chronic kidney disease, arrhythmia/atrial fibrillation, chronic pain, arthritis. The investigator's hypothesis is that patients assigned to TAU+ElderTree will have better quality of life and fewer primary care visits than those assigned to TAU+Internet.

Eligibility Criteria

Inclusion Criteria

  • are ≥65 years old
  • have been treated in the University of Wisconsin Health clinics for at least the previous 18 months with no plans to leave during the study period
  • have 3 or more of the following chronic conditions: hypertension, hyperlipidemia, diabetes, arthritis, BMI over 30, chronic kidney disease, congestive heart failure, arrhythmia/atrial fibrillation, pulmonary heart disease or pulmonary vascular disease, chronic pain, COPD
  • report no current psychotic disorder that would prevent participation
  • have no acute medical problem requiring immediate hospitalization
  • be able to read and sign the consent form in English
  • have no known terminal illness
  • be willing to share health-related study data and
  • Systolic and diastolic BP
  • Weight
  • BMI
  • HDL/LDL
  • HbA1C
  • pain score
  • lung function
  • health care utilization: number of ER visits, urgent care visits, primary care visits and specialty care visits
  • allow researchers to share information with their primary care physician
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03387735). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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