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Care4U: Self Management Intervention for Older Adult Caregivers

Not Applicable
Completed
Conditions
Cardiovascular Risk Factor
Interventions
Behavioral: Care4U
Registration Number
NCT01764399
Lead Sponsor
University of Nebraska
Brief Summary

Older adults caring for others often neglect their own health. This research is being done to see if helping caregivers focus on their own needs can improve their health and ability to care for others

Detailed Description

The specific aims are to evaluate the Care4U intervention in order to refine the intervention for a larger clinical trial, which includes 1) subject acceptability of the intervention, 2) evaluation of intervention delivery, fidelity, and data collection, and 3) evaluation of the components of the intervention (patient activation, knowledge, self-efficacy, and CV self-management strategies).

Recruitment was conducted in 2 acute care hospitals from April 2013 through Dec 2013. Six caregivers were enrolled during this time, with one dropping out after baseline.

The participants completing the study (n=5) provided data related to the aim. Four participants were able to use Adobe Connect via the provided laptops with written instructions and phone coaching. Delivery of the intervention via Adobe connect was enjoyed by the participants, with minimal connectivity problems. Participants were interested in websites and videos related to their health, but did not relate exploring these links on the laptop desktop without suggestion from the PI.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
6
Inclusion Criteria
  • Describes self as an informal Caregiver of patient who has undergone cardiac surgery (revascularization, valve, or combination)and performs ≥1 activity of daily living or instrumental activity of daily living for the patient
  • ≥ 65 years
  • Self-reports ≥1 modifiable cardiovascular risk (hypertension, hyperlipidemia, physical inactivity, obesity)
  • Lives in the same residence with patient
  • Oriented to person, place, and time (asking the subject to state their name, where he/she is (for example what building, town and state) and what time it is (time, day, date)
  • Able to hear, and speak and read English
Exclusion Criteria
  • Permanent residence in skilled or assisted care facility
  • Participation in 3 times per week exercise during the past 6 months. -

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Care4U interventionCare4UCare4U intervention with 6 weekly sessions focusing on physical activity, healthy eating, self-management, emotional responses.
Primary Outcome Measures
NameTimeMethod
Change in Physical ActivityBaseline, 6 weeks, and 3 months

Physical activity will be measured via self-report and with Actigraphy.

Secondary Outcome Measures
NameTimeMethod
Change in emotional functioning (stress, anxiety, depression)Baseline, 6 weeks, 3 months

Change in self-reported stress, anxiety and depression scores

Change in healthy diet intakeBaseline, 6 weeks, 3 months

Change in self-reported diet intake

Trial Locations

Locations (1)

Bryan Health

🇺🇸

Lincoln, Nebraska, United States

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