NCT05933564

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
110

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 28, 2023

Completed
2 days until next milestone

Study Start

First participant enrolled

June 30, 2023

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 6, 2023

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2023

Completed
Last Updated

July 6, 2023

Status Verified

June 1, 2023

Enrollment Period

6 months

First QC Date

June 28, 2023

Last Update Submit

June 28, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (1)

  • Moderating effect of cognitive reserve on the association between pain catastrophizing and cognitive function

    Baseline assessment

Study Arms (1)

Chronic Pain Patients with Varying Cognitive Reserve

Community-dwelling adults aged 65-85 years with chronic pain (≥3 months) attributable to osteoarthritis or neuropathic conditions.

Other: No intervention (cross-sectional study)

Interventions

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.

Chronic Pain Patients with Varying Cognitive Reserve

Eligibility Criteria

Age65 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of community-dwelling adults aged 65-85 years with chronic pain (≥3 months) attributable to osteoarthritis or neuropathic conditions.

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Outpatient clinic of faculty of physical therapy, Ahram Canadian University

Al Ḩayy Ath Thāmin, Giza Governorate, 3221405, Egypt

RECRUITING

MeSH Terms

Conditions

Chronic Pain

Interventions

Cross-Sectional Studies

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Epidemiologic StudiesEpidemiologic Study CharacteristicsEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Amal Fawzy, Ph.d

    Faculty of Physical Therapy, Ahram Canadian University

    STUDY DIRECTOR

Central Study Contacts

Mohamed M ElMeligie, Ph.d

CONTACT

Study Design

Study Type
observational
Observational Model
FAMILY BASED
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of Physical Therapy and Director of Electromyography Lab

Study Record Dates

First Submitted

June 28, 2023

First Posted

July 6, 2023

Study Start

June 30, 2023

Primary Completion

December 30, 2023

Study Completion

December 30, 2023

Last Updated

July 6, 2023

Record last verified: 2023-06

Data Sharing

IPD Sharing
Will not share

Locations