A Nurse-led Family-oriented Resilience Program for Caregivers of Community-dwelling Dependent Older Adults

Central South University

Status: Completed

Conditions: Caregiver Burden

Treatments: Behavioral: family resilience intervention; Behavioral: Evidence-based caregiving training; Behavioral: usual service

Study type: Interventional

Funder types: Other

Identifiers

NCT06522516

A family resilience program

Details and patient eligibility

About

This is a 3-arm controlled trial. The participants are caregivers of the community-dwelling dependent older adults. There will be around 105 participants to be recruited and randomly allocated into 3 groups. Caregiving training group will receive a evidence-based caregiving training delivered via home visit of community nurse. Caregiving training plus family resilience group will additionally receive a structured family resilience intervetion. Control group will receive usual community health care service by nurses. The primary outcomes are caregiving ability, family resilience and psychological distress, and the secondary outcomes are caregiving burden, resilience, coping, social support, and quality of life the caregivers and the older adults. The measurement will be conducted four times at baseline, after, 1-month and 3-month after intervention.

Enrollment: 105 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• ①The degree of disability of the caregiver is moderate to severe activity of daily living score above;

  • The primary caregivers are≥18 years old ;

    • The primary caregivers bear the most important care task during care, and the continuous care time are≥3 months ; -④The psychological pain thermometer score of the primary caregivers are≥5 points (the previous cross-sectional survey results showed that when the psychological pain thermometer score of the primary caregivers in disabled elderly are 5 points, the highest Youden index is obtained, and the sensitivity, specificity, positive predictive value, and negative predictive value are also high. Therefore, participants with scores above 5 points are screened as potential research subjects ); -⑤No cognitive impairment or language expression disorders; -⑥The primary caregivers have smart phones and can use them skillfully, and have access to the Internet; -⑦Voluntarily participate in this study and sign an informed consent form.

Exclusion criteria

• ①Currently participating or having received intervention from other healthcare teams within the past three months;

  • There are paid personnel such as nannies participating in the care.

    • Those who voluntarily withdrew from the research process;

      • During the research process, due to significant adverse events (such as death) involving disabled elderly individuals or primary caregivers, they were unable to continue participating in the study.

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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105 participants in 3 patient groups

Caregiving training group

Experimental group

Description:

Caregiving training group will receive an evidence-based caregiving training via manual during nurse home visit.

Treatment:

Behavioral: usual service

Behavioral: Evidence-based caregiving training

Caregiving training plus family resilience group

Experimental group

Description:

Caregiving training plus family resilience group will receive an evidence-based caregiving training and family resilience psychological intervention via manual during nurse home visit

Treatment:

Behavioral: usual service

Behavioral: Evidence-based caregiving training

Behavioral: family resilience intervention

Control group

Active Comparator group

Description:

Controlled group will receive usual community service by nurse.

Treatment:

Behavioral: usual service