A Pilot Effectiveness and Implementation Trial of CSNAT-I in Hong Kong

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe Hong Kong Polytechnic University

About this trial

In this hybrid Type 1 effectiveness-implementation pilot randomized controlled trial, 60 caregivers will be randomized into either the CSNAT-I group or usual care. Preliminary effectiveness outcomes include caregiver burden, distress, and health-related quality of life. Preliminary implementation outcomes include feasibility, fidelity, appropriateness, acceptability, cost of the intervention, as well as barriers and facilitators to intervention implementation. Quantitative data will be analyzed using descriptive analysis and linear mixed effects model, while qualitative data using thematic analysis. The CSNAT-I is expected to be preliminarily effective in improving caregiver outcomes and implementable in Hong Kong palliative care context, which will serve as the foundation for a large trial before integration into daily practice.

Eligibility criteria

Qualifiers

adults ≥18 years old;

family members taking a primary role in patient care at home as nominated by the palliative cancer patient;

ability to communicate in Chinese.

Disqualifiers

paid caregivers;

unable to complete the questionnaire due to mental impairment determined by physicians.

Trial design

Treatments tested in this trial

  • CSNAT-I

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

The Hong Kong Polytechnic University

Lead sponsor

United Christian Hospital

Collaborator

Haven of Hope Hospital

Collaborator