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Recruiting NCT06784830

NCT06784830 Nursing Interventions for Alzheimer's Patients During PET/CT Imaging

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Clinical Trial Summary
NCT ID NCT06784830
Status Recruiting
Phase
Sponsor Sichuan Provincial People's Hospital
Condition Alzheimer's Disease
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2024-06-15
Primary Completion 2025-01-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Effects on Image Quality and Patient SatisfactionAnxiety degree of patients after nursing

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 200 participants in total. It began in 2024-06-15 with a primary completion date of 2025-01-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

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.

Contact & Investigator

Central Contact

Hao Wang, Doctor

✉ 474556259@qq.com

📞 +8618313820216

Principal Investigator

Hao Wang, Doctor

STUDY DIRECTOR

Sichuan Provincial People's Hospital

Frequently Asked Questions

Who can join the NCT06784830 clinical trial?

This trial is open to participants of all sexes, studying Alzheimer's Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06784830 currently recruiting?

Yes, NCT06784830 is actively recruiting participants. Contact the research team at 474556259@qq.com for enrollment information.

Where is the NCT06784830 trial being conducted?

This trial is being conducted at Chengdu, China.

Who is sponsoring the NCT06784830 clinical trial?

NCT06784830 is sponsored by Sichuan Provincial People's Hospital. The principal investigator is Hao Wang, Doctor at Sichuan Provincial People's Hospital. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology