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NCT06557863Completed

Reducing Burden in Care Partners of Community-Dwelling Persons With Dementia and Oropharyngeal Dysphagia

Source: ClinicalTrials.gov · Last updated 1 Jun 2026

Brief summary (registry, in English)

The goal of this clinical trial is to learn if a newly-created website tool, called WeCareToFeedDysphagia, helps to reduce feelings of burden in care partners of patients with Alzheimer's disease and related dementias (AD/ADRD) who were diagnosed with trouble swallowing (oropharyngeal dysphagia). The main questions this first test (pilot) study aims to answer are: * With the data this pilot study will collect, how do we best measure how strong a relationship is between care partners who use WeCareToFeedDysphagia and reduced feelings of burden (effect size estimates)? * Is it possible (feasible) to successfully repeat this study in a larger clinical trial with more research participants? Researchers will compare a group of care partners who have access to the WeCareToFeedDysphagia tool (intervention) to a group of care partners who do not have access to the tool. Both groups will receive contact information for help from a speech language pathologist expert (enhanced usual care). Participants will: * be given access to the web tool and receive 3 text message reminders over 3 weeks to use the tool (intervention group only). * be asked to complete a remote, web-based survey three times: when enrolled in the study, at 1 month following patient leaving the hospital, and at 3 months following patient leaving the hospital.

Status (registry)
Completed
Study type
Interventional
Enrollment
80 (actual)
First submitted
14 Aug 2024
Start date
8 Oct 2024
Primary completion date
1 Aug 2025
Lead sponsor
Northwell Health
NCT number
NCT06557863

What you commit to

  • Study type: Interventional
  • Participants enrolled: 80
  • From 8 Oct 2024 to the primary completion date, 1 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Care partner of patient with a percutaneous feeding tube \[i.e. percutaneous endoscopic gastrostomy (PEG) tube, percutaneous endoscopic jejunostomy (PEJ) used exclusively\]
  • Care partner of patient who will not be discharged to the home or community setting (e.g., home, assisted living, independent living)
  • Care partner will not be involved with OD management (e.g. buying or making food, feeding, supervising) after hospital discharge

Who the study is looking for

  • Self identifies as the primary care partner of an older adult patient (patient aged 65 years or older) with Alzheimer's disease and related dementias (AD/ADRD) and oropharyngeal dysphagia (OD) admitted to the Northwell Health medicine service
  • Care partner age 18 years or older
  • Designated as the legally authorized representative (LAR) or health care proxy (HCP), or designated by the LAR or HCP to participate
  • Proficient in English
  • Has access to a device (e.g. smartphone, iPad, computer) capable of accessing a web browser

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Feinstein Institutes for Medical Research
Coordinator of this site? Confirm its status
ManhassetUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.