ArticleSpinal cord2026
Feasibility and exploratory outcomes of the COMPANION eHealth tool for the wellbeing of family caregivers of individuals with spinal cord injury.
Article in Spinal cord, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06364813 (Co-developing a Novel Intervention to Promote Wellbeing of Family Caregivers of Individuals With Spinal Cord Injury), which is not on this map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Co-developing a Novel Intervention to Promote Wellbeing of Family Caregivers of Individuals With Spinal Cord Injury
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
STUDY
designFeasibility randomized controlled trial (ClinicalTrials.gov identifier: NCT06364813).
objectivesTo evaluate the feasibility of the COMPANION eHealth tool, designed to support the well-being of family caregivers of individuals with spinal cord injury (SCI).
methodsFifty-one participants were randomized to either the COMPANION group or the control group. Participants completed a series of measures at baseline and at three and six months after baseline. Feasibility outcomes assessed process, resources, management, and treatment. The clinical outcomes reported here included caregiver burden, distress, relationship satisfaction, and caregiver competence.
resultsEight of 12 feasibility indicators satisfied predefined benchmarks. Specifically, the study protocol achieved feasibility targets for 'recruitment', 'consent', 'retention', 'assessor masking', 'Data collection: Participant & Evaluator burden', 'participant and expert burden', 'participant processing time', and 'treatment administration'. Three indicators ('treatment adherence', 'Platform and Internet stability', and 'dose-level response') fell short of their respective benchmarks mainly due to measurement or technical limitations, while a fourth ('perceived usability') fell below because participants reported lower anticipated future use. There were no statistically significant differences between the two groups.
conclusionsOur findings provide some support for the feasibility of the study protocol for evaluating COMPANION. However, 'treatment adherence', 'Platform and Internet stability', and 'dose-level response' require attention. The findings regarding anticipated future use suggest the need to employ strong engagement strategies, such as a peer support component and reminders, to keep participants engaged with COMPANION. Moreover, it is possible that COMPANION was more beneficial for newer caregivers than for more experienced caregivers.
Identifiers
42816541What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.