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Investigation of the influence of a moderate pain stimulus on parameters of the pupillary light reflex and on the respiratory air composition and their correlation with psychosocial stress tolerance

Investigation of the influence of a moderate pain stimulus on parameters of the pupillary light reflex and on the respiratory air composition and their correlation with psychosocial stress tolerance

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00034895
Enrollment
30
Registered
2024-08-29
Start date
2024-10-28
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

No diseases/health problems are examined

Interventions

Group 1: 30 participants. All participants are medical examined before start of the test session. All participants are examined in an approx. 60-minute lasting session. In test cycle A, after a dark

Sponsors

Uniklinik RWTH Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: - healthy subjects (n=30) - written informed consent - Participation in study "Differential effects of perseverative cognition on recovery from acute stress in a virtual reality environment" (EK 23-320)

Exclusion criteria

Exclusion criteria: - Participants with epilepsy, diseases of the peripheral nerves or other neurological diseases (e.g., migraine, post-apoplexy, cerebral hemorrhage, neurodegenerative diseases) - Particiants with severe eye diseases (e.g. glaucoma, retinal detachment, pupillary motor disorders) - Patients with mental illnesses - Participants with metabolic disorders (e.g. diabetes mellitus) - Participants who are taking medication that affects their ability to react and concentrate (e.g. painkillers from level II according to WHO) - Drug and/or alcohol abuse - Visible head injuries or diseases in the area of the head - Artificial eye lenses or the absence of an eye lens - Pregnant, breastfeeding and underage test subjects (< 18 years) - Skin diseases or sensory disorders of the feet - Polyneuropathy - Severe peripheral arterial occlusive disease - Raynaud's syndrome - Persons with syncope - Persons suffering from respiratory diseases (asthma)

Design outcomes

Primary

MeasureTime frame
The primary objective is to test the predictability of the individual stress response to psychosocial stress by assessing the parameters of the PLR under a cold-induced moderate pain stimulus (ice bath) compared to a warm foot bath.

Secondary

MeasureTime frame
The secondary aim of the present study is to investigate whether induced acute stress (pain stimulus) can be identified by breath analysis and whether VOCs and/or NO have the potential to act as biomarkers that both recognize and differentiate stress.

Countries

Germany

Contacts

Public ContactMichael Kursawe

Uniklinik RWTH Aachen

mkursawe@ukaachen.de+492418088544

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026