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Effect of MIST on Esophageal Sensitivity in HV

Effect of Acute Psychosocial Stress on Esophageal Sensitivity in Healthy Volunteers

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05427188
Acronym
MIST
Enrollment
24
Registered
2022-06-22
Start date
2022-06-30
Completion date
2022-10-31
Last updated
2022-06-22

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

Conditions

Stress

Brief summary

Effect of acute psychosocial stress on esophageal sensitivity in healthy volunteers.

Detailed description

Gastro-esophageal reflux disease (GERD), defined as the presence of symptoms or lesions that can be attributed to the reflux of gastric contents into the esophagus, is an increasingly prevalent condition in Western societies. The most typical symptoms are heartburn and regurgitation, however GERD can also manifest itself through a variety of other esophageal and extra-esophageal symptoms (e.g. chronic cough). GERD patients can be divided into different categories based on upper endoscopy and pH or impedance-pH (MII-pH) monitoring. In the absence of lesions (esophagitis) during upper endoscopy, a pH or MII-pH monitoring will be performed. A first subcategory are patients with true GERD, characterized by an abnormal acid exposure and a positive or negative symptom association. The second and third category are patients with reflux hypersensitivity (RHS) and functional heartburn (FH)characterized by normal acid exposure on the MII-pH monitoring and a positive and negative symptom reflux association, respectively. The basis for symptom generation/perception in GERD patients is not yet completely understood, but different mechanisms have been proposed including esophageal hypersensitivity, in which psychosocial stress is considered as a potential factor. This was shown in a study where 64% of the participants with heartburn reported that psychological factors, such as life stress, aggravate their symptoms. Furthermore, Fass et al. observed that auditory stress exacerbated symptom perception during esophageal acid perfusion (6). Moreover, our group investigated the effect of intravenous corticotrophin releasing hormone (CRH) on esophageal in healthy volunteers and showed that CRH is able to increase esophageal sensitivity to mechanical distention. Nevertheless, these previously performed studies in patients have some limitations: no measurable increase in cortisol (hypothalamo-pituitary-adrenal (HPA)-axis was not affected in these studies) and patients with RHS and FH - in whom the effect of stress is hypothesized to be the most relevant - were not included. To induce moderate psychologic stress in the current study, the Montreal Imaging Stress Task (MIST) will be used. During this protocol, participants receive mental arithmetic challenges, together with social evaluative threat components from the program and/or the investigator (sham condition: threat components from the program and/or the investigator are absent). This MIST protocol can be used when investigating the effects of perceiving and processing psychosocial stress in the human brain in functional imaging studies. Therefore, we want to investigate the relation between sensitivity to different stimuli (esophageal sensitivity) and psychosocial stress in healthy volunteers and patients (True GERD, RHS and FH).

Interventions

BEHAVIORALStress paradigm

HV will receive mental arithmetic challenges, together with social evaluative threat components from the program and/or the investigator

BEHAVIORALSham paradigm

HV will receive mental arithmetic challenges where threat components from the program and/or the investigator are absent

Sponsors

Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Aged between 18 to 65 years. All participants will receive and sign a copy of the informed consent before initiation of the study.

Exclusion criteria

* A history of any upper gastrointestinal (GI) symptoms, complaints or diseases; * Prior history of esophageal or gastric surgery or endoscopic anti-reflux procedure; * Psychiatric disorders; * Concomitant use of other medication or treatments except for oral contraceptives; * Use of medication altering GI motility; * Pregnant or nursing women; * History of drugs or alcohol abuse.

Design outcomes

Primary

MeasureTime frameDescription
Esophageal mechanical sensitivityWill be assessed at time point 180 minutesChange in balloon distention
Esophageal chemical sensitivityWe be assessed at time point 180 minutesChange in time for reaching pain threshold

Secondary

MeasureTime frameDescription
Cortisol levelsevery 15 minutes a saliva sample during 4.5 hours: at time points (in minutes) 0, 15, 30, 45, 60, 75, 90, 105, 120, 135, 150, 165, 180, 195, 210, 225, 240, 255, 27Change in cortisol levels

Countries

Belgium

Contacts

Primary ContactAnnelies Geeraerts
annelies.geeraerts@kuleuven.be+321643385

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026