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Recruiting NCT06784830

Nursing Interventions for Alzheimer's Patients During PET/CT Imaging

No phase Interventional Alzheimer's Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Effects on Image Quality and Patient Satisfaction, Anxiety degree of patients after nursing.
Who it may be relevant to
Registry conditions: Alzheimer's Disease. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Enhancing Nursing Interventions for Alzheimer's Patients During PET/CT Imaging: Effects on Image Quality and Patient Satisfaction

Overview

The impact of nursing Interventions during PET/CT imaging in Alzheimer's patients on image quality and patient satisfaction will be assessed in 200 patients.

Detailed description

This study will analyze clinical data from 200 Alzheimer's disease (AD) patients who underwent PET imaging and were admitted to Sichuan Provincial People's Hospital over a period of six months. The control group will receive routine nursing intervention, while the observation group will receive a refined specialized nursing intervention. We will meticulously compare various performance aspects in both groups to assess the impact of refined specialized nursing intervention on patients' image quality and patient satisfaction.

Interventions

  • Other Effects on Image Quality and Patient Satisfaction
    Effect of nursing intervention on image quality and patient satisfaction during PET/CT imaging in Alzheimer's patients
  • Other Anxiety degree of patients after nursing
    Self Rating Anxiety will be used Scale (SAS) to assess the degree of anxiety after care

Primary outcome measures

  • Comparison of refined nursing and routine nursing intervention in Alzheimer's Patients during PET/CT Imaging [Time frame: through study completion, an average of 6 months]

Eligibility criteria

Inclusion criteria

  • Meet the criteria for diagnosing dementia as described in the fourth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-R), Use the diagnostic criteria for AD from the National Institute of Neurology, Speech and Communication Disorders and Stroke - Alzheimer's Disease and Related Disorders (NINCDS-ADRDA) or the National Institute on Aging and Alzheimer's Disease Association (NIA-AA).

Exclusion criteria

  • Patients with a history of stroke and focal neurological signs, and imaging findings consistent with small cerebral vascular disease (Fazekas score ≥2);
  • The presence of other neurological disorders that can cause brain dysfunction (e.g., depression, brain tumors, Parkinson's disease, metabolic encephalopathy, encephalitis, multiple sclerosis, epilepsy, brain trauma, Normal facial pressure hydrocephalus);
  • The presence of other systemic diseases that can cause cognitive impairment (such as liver insufficiency, renal insufficiency, thyroid dysfunction, severe anemia, folic acid or vitamin B12 deficiency, syphilis, HIV infection, alcohol and drug abuse, etc.);
  • There is mental and neurological retardation.
  • There are other diseases that are known to cause cognitive impairment.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

China · 1 center
  • Departments of Nuclear Medicine, Sichuan Provincial People's Hospital — Chengdu

Identifiers

NCT: NCT06784830 · SichuanPPH-HL

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗