Overview
The purpose of the present study is to conduct a two-arm Randomized Control Trial (RCT) comparing individuals receiving the 90Second Caregiver health letter, with a usual care (routine care received by caregivers) control group.
The goals of the present study are:
- To evaluate the effectiveness of the 90Second Caregiver health letter in improving caregiver's self-efficacy (primary outcome), savouring, and quality of life (secondary outcomes).
- To evaluate the effectiveness of the 90Second Caregiver health letter in reducing caregiver's psychological strain and caregiver burden (secondary outcomes).
- To examine the impact of levels of engagement with the 90Second Caregiver health letter on primary and secondary outcomes.
- To assess the usability of the 90Second Caregiver health letter, as it relates to the relevance of topic, user friendliness, and appropriateness of the readability levels.
- To evaluate psychometric properties of self-constructed measures in 90Second newsletter.
Description
The present study will examine the effectiveness of the 90Second Caregiver health letter in increasing self-efficacy in a sample of informal caregivers of ABI survivors in Nova Scotia. Participants in this study will be recruited from the Caring Forward Trials within Cohort Study (REB#1025253). The study is funded by the Nova Scotia Department of Health and Wellness.
Eligibility
Inclusion Criteria:
- Participant is currently enrolled in the Caring Forward Trials within Cohort study (REB#1025253)
- Participant has agreed to be contacted for future studies by Dr. McGrath's staff
- Participant has agreed for their data to be used for future studies
- Participant has mild levels of distress, as indicated by mild scores on the DASS-21 and/or the ZBI-SF
Exclusion Criteria:
- Participant is NOT currently enrolled in the Caring Forward Trials within Cohort study (REB#1025253)
- Participant has NOT agreed to be contacted for future studies by Dr. McGrath's staff
- Participant has NOT agreed for their data to be used in future studies
- Participant does NOT report mild levels of distress, as indicated by mild scores on the DASS-21 and/or the ZBI-SF