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Determinants of stress and relaxation:effects of orange odor

Determinants of stress and relaxation:effects of orange odor - Determinants of stress and relaxation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34694
Enrollment
156
Registered
2010-03-22
Start date
2010-04-07
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

stress en angst, niet in een klinische context, dus normale stressvorming bij gezonde personen Stress

Interventions

In order to induce stress, the Trier Social Stress Test will be administered: Participants will be asked to give an oral presentation to an expert panel of judges, followed by a sequential arithmeti

Sponsors

Universiteit Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Students who are generally healthy, between 18-25 years of age, do not have a psychiatric condition specifically an anxiety disorder or post-traumatic stress disorder, who are not pregnant or possibly pregnant, who have a good (self-reported) sense of smell, no severe allergies, no asthma, will be included in the study. Participants will not be on any prescribed medications other than oral contraceptives. Participants who have a severe cold or the flu at the time of the lab visit will be rescheduled.

Exclusion criteria

Exclusion criteria: Students who indicate not to be healthy in general, are below 18 years or above 25, to have a psychiatric condition, or, specifically an anxiety disorder or post-traumatic stress disorder, low-average sense of smell, to be pregnant or possibly pregnant, to have severe allergies or asthma will be excluded from the study. Orange odor may have anxiolytic or sedative effects. Participants who are on prescribed medications will be excluded from the study. We will not check whether these are anxiolytics or sedatives in order not to invade the participant*s privacy too much (advice of M.D. involved in study, Dr. Klopping-Ketelaars). There is no specific reason for excluding pregnant women in the sense that this procedure is potentially harmful for pregnant women (or the unborn foetus), but we think it is undesirable to expose pregnant women to undue stressors.

Design outcomes

Primary

MeasureTime frame
The main endpoints are salivary cortisol (psychophysiological) as direct measure of social, autonomic stress, and self-reported stress and anxiety.

Secondary

MeasureTime frame
The secundary endpoints are skin conductance response and heart rate as measures of autonomic stress, and mood.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)