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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05933564
Other study ID # 012/20265888
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 30, 2023
Est. completion date December 30, 2023

Study information

Verified date June 2023
Source Ahram Canadian University
Contact Mohamed M ElMeligie, Ph.d
Phone +201064442032
Email mohamed.elmeligie@acu.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To investigate the association between cognitive reserve, pain catastrophizing, and cognitive function in geriatric patients with chronic pain, and to explore whether cognitive reserve moderates the relationship between pain catastrophizing and cognitive function.


Recruitment information / eligibility

Status Recruiting
Enrollment 110
Est. completion date December 30, 2023
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 65 Years to 85 Years
Eligibility Inclusion Criteria: - Aged 65 to 85 years - Experiencing chronic pain (=3 months) attributable to osteoarthritis or neuropathic conditions - Able to read, write, and speak the language in which assessments are administered - Willing and able to provide informed consent Exclusion Criteria: - Diagnosed with a neurodegenerative disorder (e.g., Alzheimer's disease, Parkinson's disease) - History of significant head injury, stroke, or brain tumor - Current substance abuse or dependence - Severe psychiatric illness (e.g., schizophrenia, bipolar disorder) - Significant sensory or motor impairments that may interfere with the ability to complete assessments

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention (cross-sectional study)
This is a cross-sectional study examining the association between cognitive reserve, pain catastrophizing, and cognitive function in geriatric patients with chronic pain; no intervention is being implemented or tested.

Locations

Country Name City State
Egypt Outpatient clinic of faculty of physical therapy, Ahram Canadian University Al ?ayy Ath Thamin Giza

Sponsors (1)

Lead Sponsor Collaborator
Ahram Canadian University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Association between pain catastrophizing and cognitive function he relationship between pain catastrophizing, as measured by the Pain Catastrophizing Scale (PCS), and cognitive function, as measured by the Montreal Cognitive Assessment (MoCA version 7.1). Baseline assessment
Secondary Moderating effect of cognitive reserve on the association between pain catastrophizing and cognitive function Investigate whether cognitive reserve, as measured by the Cognitive Reserve Index Questionnaire (CRIq), moderates the relationship between pain catastrophizing (PCS) and cognitive function (MoCA version 7.1). Baseline assessment
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