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HomeClinical Trial & PipelineAlzheimer's & DementiaNCT07779863: Acupressure as Long-term Intervention to Slow the Progression of Early/Mild Alzheimer's Disease
ClinicalTrials.gov (NIH/NLM)Alzheimer's & DementiaClinical Trial & PipelineFAIR Metadata / API
NLM Public Domain Open Registry

NCT07779863: Acupressure as Long-term Intervention to Slow the Progression of Early/Mild Alzheimer's Disease

November 6, 2026
The University of Hong Kong
On This Page:Specs MatrixSummary & AbstractDeep Research BriefData Access & CodeCitations & Related

Study Design & Technical Specifications

Sample Size / Cohort

188 Participants

Subject / Study Model

Human Clinical Cohort

Analytical Modalities

Clinical Trial ProtocolNATherapeutic Intervention

Primary Abstract & Repository Description

Source: ClinicalTrials.gov (NIH/NLM)
This is an assessor-blinded, randomized controlled trial. A total of 188 older adults aged 60-85 years with early/mild Alzheimer's disease (AD) will be recruited from care and attention homes for the elderly and elderly activity centres. They will be randomly assigned to receive least acupressure control (LAC, n = 94) and Comfy Acupressure for the Elderly (CAE, n = 94), administered by caregivers (i.e., trained research assistants), for 3 sessions a week for 12 months. The primary outcome is the change in the Montreal Cognitive Assessment, Hong Kong version (HK-MoCA) score from baseline. The secondary outcomes include functional independence, psychological well-being, sleep quality, and health-related quality of life. The outcomes will be assessed at baseline and once bimonthly thereafter, totalling 7 sessions. A linear mixed-effect model will be applied to compare the primary and secondary outcomes. Three blood samples will be collected at baseline, 6 months, and 12 months, respectively, and the baseline blood sample will be immediately measured for the measurement of plasma Aβ42, Aβ40, p-tau181, and , blood glial fibrillary acidic protein () and neurofilament light ch...
CNS Open Data Deep Research Brief

Editorial Critique, Methodological Value & Reusability Guide

Structured via CNS Domain Knowledge Engine

1. Scientific Context & Premise

Primary Premise (ClinicalTrials.gov (NIH/NLM)): "This is an assessor-blinded, randomized controlled trial." Within Alzheimer's Disease (AD), this work examines NCT07779863, NA, NOT YET RECRUITING, Comfy Acupressure for the Elderly, Least acupressure control in relation to Aβ42/40, p-tau217, p-tau181, GFAP, NfL, and APOE ε4 genotype interactions. Authored by The University of Hong Kong.

2. Study Architecture & Findings

Study Architecture: Human Clinical Cohort (188 Participants) utilizing Clinical Trial Protocol, NA, Therapeutic Intervention. Reported quantitative parameters in the abstract include: 85 years; n = 94; 3 sessions; 12 months. Key reported conclusion: "Three blood samples will be collected at baseline, 6 months, and 12 months, respectively, and the baseline blood sample will be immediately measured for the measurement of plasma Aβ42, Aβ40, p-tau181, and p-tau217, blood glial fibrillary acidic protein (GFAP) and neurofilament light ch..."

3. Secondary Analysis & Reusability

Secondary Analysis Applications: (1) Cross-referencing Clinical Trial Protocol, NA, Therapeutic Intervention variables (NCT07779863, NA, NOT YET RECRUITING, Comfy Acupressure for the Elderly, Least acupressure control) against open repositories in Alzheimer's Disease (AD); (2) Benchmarking feature distributions and effect sizes reported in "NCT07779863: Acupressure as Long-term Intervention to Slow the Progression of Ea"; (3) Informing cohort stratification and endpoint selection.

4. Methodological Caveats & Governance

Methodological Note: When integrating these Clinical Trial Protocol, NA, Therapeutic Intervention findings, account for cohort-specific inclusion criteria (188 Participants), potential site/instrument batch effects, and repository license terms (NLM Public Domain Open Registry).

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Data Access, Reproducibility & Analysis Starter Guide

FAIR Open Science & Clinical Metadata Verification Protocol

FAIR Metadata / API

Quick Data Access & Structured Export

Open the primary repository directly or download structured metadata (JSON / CSV) in one click.

Open Primary Data (ClinicalTrials.gov (NIH/NLM))Download Data

This resource is indexed under FAIR (Findable, Accessible, Interoperable, and Reusable) open-science metadata standards, enabling programmatic cross-referencing across Europe PMC, Semantic Scholar, ClinicalTrials.gov, and CNS Open Data.

Programmatic Data Retrieval (Python Starter Code & Recommended SDKs)

Python Quickstart: Query Europe PMC & Semantic Scholar Metadata

# Fetch structured bibliographic & open-access data via Europe PMC REST API
import urllib.request
import urllib.parse
import json

query = "NCT07779863: Acupressure as Long-term Intervention to Slow the Progression of Ea"
url = f"https://www.ebi.ac.uk/europepmc/webservices/rest/search?query={urllib.parse.quote(query)}&format=json&resultType=core"

with urllib.request.urlopen(url, timeout=10) as response:
    payload = json.loads(response.read().decode("utf-8"))
    results = payload.get("resultList", {}).get("result", [])
    if results:
        record = results[0]
        print("Title:", record.get("title"))
        print("Journal / Source:", record.get("journalTitle") or record.get("bookOrReportDetails"))
        print("Cited By Count:", record.get("citedByCount", 0))

Recommended Open-Source Software & SDKs

NiBabelPython SDK

Read and write access to NIfTI, GIFTI, and BIDS neuroimaging file formats in Python.

Scanpy (scverse)Python / AnnData

Scalable Python toolkit for analyzing AnnData (.h5ad) single-cell gene expression matrices.

Standardized 4-Step Workflow & Governance Checklist

Standardized Acquisition & Preprocessing Workflow

1. Programmatic Metadata & Full-Text OA Retrieval

Query Europe PMC or Crossref REST APIs using the persistent DOI/URL to retrieve structured XML full text, supplementary tables, and grant links.

2. Study Design & Cohort Eligibility Screening

Extract sample size, inclusion/exclusion criteria, and primary outcome endpoints for systematic review (PRISMA) inclusion.

3. Data Availability & Supplementary Repository Linkage

Locate accession numbers (GEO, SRA, OpenNeuro, DANDI, Zenodo, Figshare) referenced in the Data Availability section.

4. Citation Graph & Replication Tracking

Monitor supporting and contrasting citations over time to verify whether key findings have been independently replicated.

Reproducibility & Governance Checklist

  • Verify whether the source is a peer-reviewed journal publication or an unrefereed preprint before clinical citation.
  • Check supplementary data licenses (CC-BY / CC0) when extracting figures or summary statistics for meta-analyses.
  • Cross-reference NCT clinical trial identifiers when evaluating therapeutic efficacy or biomarker endpoints.

Tags & Modalities

Clinical Trial ProtocolNATherapeutic Intervention#NCT07779863#NA#NOT YET RECRUITING#Comfy Acupressure for the Elderly#Least acupressure control

Bibliometrics, Peer-Review Status & Citation Export

Cross-referenced via Semantic Scholar, Europe PMC & bioRxiv

1. Citation Metrics & Context Breakdown

0
Total Citations
0
Influential Citations

Citation Context Breakdown

Citation intent breakdown (Supporting vs. Contrasting) is currently accumulating in Semantic Scholar for this record. Researchers reusing this resource should cite the primary DOI/URL using the standardized formats below.

2. Peer-Review Validation & Revision History

Verified Publication / Open Dataset Record

Metadata and license integrity verified against primary repository records.

3. Standardized Academic Citation & BibTeX Export

Selected Format (APA)
The University of Hong Kong (2026). NCT07779863: Acupressure as Long-term Intervention to Slow the Progression of Early/Mild Alzheimer's Disease. ClinicalTrials.gov (NIH/NLM). https://clinicaltrials.gov/study/NCT07779863
BibTeX Entry (LaTeX / Reference Managers)
@article{kong2026ctgo,
  title = {NCT07779863: Acupressure as Long-term Intervention to Slow the Progression of Early/Mild Alzheimer's Disease},
  author = {The University of Hong Kong},
  year = {2026},
  journal = {ClinicalTrials.gov (NIH/NLM)},
  howpublished = {\url{https://clinicaltrials.gov/study/NCT07779863}},
  doi = {},
  note = {CNS Open Data: alzheimer}
}

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This page provides structured scientific metadata, methodological critiques, and open-data reusability guidelines intended strictly for neuroscience researchers and data scientists. It does not constitute medical advice, clinical diagnosis, or treatment recommendations.

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