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N/A Completed N=82 Randomized Single-blind Supportive Care

Building a Bridge (BAB) Between Clinical and Community Care

Source: ClinicalTrials.gov NCT03932812 ↗
Enrolled (actual)
82
Serious AEs
0.0%
Results posted
Dec 2022
Primary outcomePrimary: Modified Zarit Burden Interview — 19.429; 17.950; 32.207; 27.160 Burden score — p=0.206

Summary

Dementia diagnosis triggers a transitional phase for the individuals and their families, often causing emotional distress and family conflicts due to the ambiguity of the illness and future trajectories. Families often report a lack of information and guidance during the period immediately following diagnosis, suggesting a missed opportunity for prevention of family distress at the outset of the caregiver and patient career. With large and increasing numbers of individuals newly diagnosed with Alzheimer's Disease and Related Dementias (ADRD) each year, there is an urgent need to develop effective intervention models to support role transitions and minimize distress related to ADRD diagnosis. The long-term goal of this research is to minimize negative consequences of ADRD by enhancing the support systems of the affected families as they start their new and challenging phase of life as patients and family caregivers. The aim of this research is to evaluate the impact of this new Options Counselor-Health Education (OC-HE) intervention on bridging the medical and community-settings through potential mechanisms of influence, enhancement of social networks and support. Implementation strategies will be developed in collaboration with partnering clinics and local Area Agencies on Aging. Participants will be recruited from three clinics at the University of Iowa Hospitals and Clinics (UIHC) that provide dementia diagnostic services and randomized into an intervention or control arm; and complete baseline and three- and six-month follow-up interviews. This study is innovative in its consideration of contributing factors at multiple levels of the ecological model (i.e., individual, social network, and organizational) and its collaborative approach, involving medical clinics, an Area Agency on Aging (AAA), and Alzheimer's Association (AA) to develop and evaluate a new care model that bridges between the medical and community settings.

Outcome Measures

OutcomeResultp-value
PRIMARY
Modified Zarit Burden Interview
19.429; 17.950; 32.207; 27.160; 31.375; 28.615 0.206
SECONDARY
Knowledge of Formal Services
25.381; 25.350; 29.690; 28.154; 29.520; 28.222 0.101
SECONDARY
Center for Epidemiologic Studies Depression
4.051; 2.806; 19.517; 19.640; 7.240; 5.815 0.836
SECONDARY
Emergency Care Use
0.714; 0.750; 0.207; 0.320; 0.292; 0.346 0.567
SECONDARY
Social Network-Uplift
11.439; 10.750; 8.448; 12.400; 7.880; 9.889 0.014 sig
SECONDARY
Social Network-Malfeasant
2.098; 1.800; 4.966; 8.360; 1.520; 0.852 0.010 sig

Eligibility Criteria

Inclusion Criteria

  • 18 years of age
  • Speaks English
  • Lives in Iowa
  • Caregiver of someone diagnosed with dementia within the past 6 months

Exclusion Criteria

  • Does not meet inclusion criteria
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03932812). 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. Informational only — not medical advice.

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