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An E-health Letter Intervention for Caregivers

An E-health Letter Intervention for Caregivers

Non Recruiting
18 years and older
All
Phase N/A

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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

Study details
    Caregivers
    Acquired Brain Injury

NCT05882461

IWK Health Centre

20 August 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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