Pilot Testing Dementia-Enhanced Training and Tool for Home Hospice Clinicians
該当なし
完了
NCT05719077
| 対象疾患 | Alzheimer's Disease and Related Dementias |
|---|
| 相 | 該当なし |
|---|
| スポンサー | Rutgers, The State University of New Jersey |
|---|
| ステータス | 完了 |
|---|
| 参加者数 | 93 名 |
|---|
| 介入(薬剤) | EDITH-HC |
|---|
| 開始日 | 2023年10月6日 |
|---|
| 完了日 | 2025年6月30日 |
|---|
| 結果公開日 | 2026年7月16日 |
|---|
概要
The purpose of this study is to pilot test the feasibility, acceptability, and preliminary efficacy of a clinically useful, inclusive dementia-enhanced training and tool for use by home hospice clinicians to improve care and support for Black and White patients with dementia and their family caregivers. The investigators expect family caregivers of clinicians in the intervention group will report less caregiver burden (primary outcome) than caregivers of clinicians in the control group. The investigators expect that, compared to clinicians in the control group (usual care), clinicians in the intervention group (receive the training and use the tool) will demonstrate more knowledge of dementia-related caregiving issues (secondary outcomes). In exploratory analyses, the investigators expect family caregivers will report greater self-efficacy and preparedness, and that patients of clinicians in the intervention group will experience fewer live discharges than family caregivers of patients of clinicians in the control group.
Family Caregiver Burden
Baseline and through first subsequent hospice visit, an average of 8 weeks · change in score on a scale
| Intervention Family Care Partners (FCP) | -1.0 ± 3.5 change in score on a scale |
|---|
| Control Family Care Partners | 0.4 ± 4.6 change in score on a scale |
|---|
BENITIONS で見る
ClinicalTrials.gov の原文を見る
同じ疾患の他の治験
すべての治験
このページは ClinicalTrials.gov の公開データをまとめたものです。医学的助言ではなく、投資助言でもありません。必ず専門医にご相談ください。