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Clinical Trials/NCT06636253
NCT06636253
Recruiting
Not Applicable

Does Stress Change EEG Measures in Students: A Feasibility Study.

Scotland College of Chiropractic1 site in 1 country10 target enrollmentOctober 15, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Electroencephalogram
Sponsor
Scotland College of Chiropractic
Enrollment
10
Locations
1
Primary Endpoint
Feasibility recruitment rates
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Psychological stress is a frequent human affection and has a considerable impact on modern society, and tertiary-level students often report increased stress levels as the semester progresses. While many questionnaires assess psychological stress, they do not capture objective data. Much research has shown that electroencephalography (EEG) can capture objective markers of stress, and recent studies have shown that EEG can even classify stress levels.

This study aims to assess the feasibility of using EEG to objectively assess stress over the course of a semester of work in chiropractic students engaged in a Masters level course in Scotland.

Detailed Description

The study's primary aim is to assess the feasibility of a more extensive future study. The investigators also hypothesise that as the semester progresses, participants will exhibit changes in their EEG outcomes that may be related to longitudinal or direct stressors. Study design and setting This study will be an observational study with a stress-related questionnaire (Depression, Anxiety, and Stress Scale - 21 (DASS-21)) over three time-points. Participants The investigators aim to recruit 10 participants and assess them three times over the course of their semester, early, middle, and late semester, with at least a four-week gap between each data collection. The investigators aim to recruit only healthy Scottish chiropractic students with no prior diagnosed mental disorder and who are capable of understanding the study procedure. Procedure Following screening for eligibility and consent, i.e., visit one (baseline), participants will be asked to answer a questionnaire and undergo EEG measurement and Montreal imaging stress task (MIST). The same EEG and questionnaire procedure will be performed in the remaining two data collection sessions. Each EEG recording session, with the participant seated, will consist of a two-minute resting state with the eyes closed for a baseline relaxation level among the participants. A following two-minute eyes-open phase will take place. After which, participants will be asked to perform the experimental phase of the MIST task, a following two-minute recording phase will be with the eyes open, and a final two-minute resting phase with eyes closed will conclude the task. The investigators aim to conclude the data collection around 16 weeks after the initial participant is recruited.

Registry
clinicaltrials.gov
Start Date
October 15, 2024
End Date
June 1, 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Scotland College of Chiropractic
Responsible Party
Principal Investigator
Principal Investigator

Alice Cade

Senior lecturer and research fellow

Scotland College of Chiropractic

Eligibility Criteria

Inclusion Criteria

  • Healthy Scottish chiropractic students with no prior diagnosed mental disorder and who are capable of understanding the study procedure.

Exclusion Criteria

  • A pre-diagnosed mental health disorder

Outcomes

Primary Outcomes

Feasibility recruitment rates

Time Frame: 0, 6, 12 weeks

recruitment rates - how many people were recruited ove rthe study time period

Feasibility - retention

Time Frame: 0, 6, 12 weeks

Participant retention - how many participants completed the full study

Feasibility - queries

Time Frame: 12 weeks

queries from participants - how many question did participants ask and were they answerable

Feasibility - ease

Time Frame: 12 weeks

Ease of data collection - was the data collection procedure manageable for the investigator

Feasibility - Adverse

Time Frame: 12 weeks

Adverse events - were any adverse events either minor or significant, recorded at any time throughout the trial

Secondary Outcomes

  • Electroencephalogram recordings(12 weeks)

Study Sites (1)

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