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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03709238
Other study ID # UAarhus_Susan
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 3, 2019
Est. completion date August 31, 2021

Study information

Verified date May 2021
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study investigates pain processing and pain reporting in patients with Alzheimers disease compared to healthy participants. Employing a within-subject design, the study includes patients with Alzheimers disease and healthy participants that are exposed to thermal stimuli. During the test session the facial expressions of the participant are video recorded. By repeating this on separate test days, the involvement of pain relief and pain increase is investigated.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date August 31, 2021
Est. primary completion date August 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - Mild to moderate patients with Alzheimers disease (group 1) - Healthy participants ( group 2) Exclusion Criteria: - Chronic pain conditions - Other medical, psychiatric or neurological disorders - Use of pain-reliving medication 24 hours prior to testing

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Thermal stimulation
Thermal stimulation

Locations

Country Name City State
Denmark Department of Psychology and Behavioural Sciences Aarhus Midtjylland

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numerical rating scale (NRS) Acute pain assessed on numerical rating scale from 0 (no pain experience) to 10 (worst pain), examining pain intensity. The participant will provide a number on the scale which reflects their pain intensity. Participants will be tested on three different days. The numerical rating scale will be applied after each thermal stimulus for each test session.
Secondary Pain Assessment in persons with Impaired Cognition (PAIC) Video recordings will be analyzed with the PAIC scale from 0 (not at all) to 3 (great degree). Participants will be video recorded on each of the three test days during testing.
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