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Completed

NCT Number: NCT06414252

Social Evaluated Cold Pressor Test in Hereditary Angioedema Patients

This study aims to evaluate the differences in objective and subjective stress responses between patients with hereditary angioedema and healthy individuals to a stress-induced challenge like socially-evaluated cold pressure test. The study also investigates the role of psychological variables in influencing the stress response.

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Key information

About this study

Stressful encounters, ranging from daily hassles to major life events, are ubiquitous in our everyday lives and are often responsible for significant changes in affective and cognitive processes. In various physical diseases, including hereditary angioedema (HAE) due to C1 inhibitor deficiency, stressful events are also frequently reported by patients to trigger acute attacks. These include physical stress (such as injury, pain, viral infections, medical and dental procedures, and surgery) and mental stress (including stress from life events and school or work, clinical depression, and anxiety), or stress originating from the disease itself, especially if the disease is characterized by an unpredictable nature like HEA that directly impacts patients' choices in everyday life. Available literature related to the link between HAE and stress is limited and mainly focused on the patients' narratives. Self-reported data suggested that the main HAE trigger seems to be stress, followed by physical trauma. These observations suggest analyzing the perceived psychological effects consequent to stress exposure together with biochemical and physiological responses. The effect of stress could be systematically examined in a laboratory environment using a standardized protocol that reliably induces stress and activates major stress responses in experimental contexts. A reliable test to induce stress in HAE patients combining these two aspects may be the Socially Evaluated Cold Pressor Test (SECPT). SECPT is an extension of the classical Cold Pressor Test, in which participants immerse one of their hands in ice water with socio-evaluative elements, and has been proven to be a highly efficient tool for experimental stress induction in humans. Adding social-evaluative elements to the original physical stress boosted the cortisol response, making the SECPT a well-established standard protocol in human stress research that may represent an efficient alternative to other established protocols, such as the Trier Social Stress Test, a 'gold standard' in the field. A recent review confirmed that exposure to the SECPT leads to changes in subjective feeling, and triggers a significant sharp increase in systolic and diastolic blood pressure. The present study aims to evaluate objective and subjective stress responses between HAE patients and healthy controls due to SECPT. Moreover, as secondary aims, the study wants to investigate if the presence of anxiety and depressive symptoms, as well as body appreciation, trust in the body, pain catastrophizing, pain interference, and pain intensity, affect or mediate stress response in patients and healthy subjects similarly or differently.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Documented diagnosis of hereditary angioedema due to C1 inhibitor deficiency aged between 18 and 65 years (for the group of patients)

Exclusion criteria

  • Any type of chronic disease requiring chronic treatment (i.e. hypertension, previous myocardial infarction, diabetes, chronic heart failure, autoimmune disease, neurodegenerative disease)
  • Active acute disease;
  • Sars-Cov2 infection in the previous 3 months.
  • An acute attack experienced within the previous week and within 72 hours after the registration (a posteriori exclusion).

Treatment and study plan

Primary outcomes

  1. Heart rate

    Time frame: Baseline

    Changes in the heart rate (beats per minute) from resting to SECPT condition

  2. Systolic arterial pressure

    Time frame: Baseline

    Changes in the systolic blood pressure (mmHg) from resting to SECPT condition

  3. Diastolic arterial pressure

    Time frame: Baseline

    Changes in the systolic blood pressure (mmHg) from resting to SECPT condition

  4. Visual Analogue Scale of perceived stress

    Time frame: Baseline

    Changes in the perceived stress due to SECP. Scores ranges from 0 (no stress) to 100 (worst stress possible)

  5. Concentration of inflammatory cytokines

    Time frame: Baseline

    Changes in the concentration of inflammatory cytokines (pg/ml) due to SECPT

  6. Concentration of plasma cathecolamines

    Time frame: Baseline

    Changes in the concentration of plasma cathecolamines (pg/ml) due to SECPT

Secondary outcomes

  1. Hospital Anxiety and Depression Scale

    Time frame: Baseline

    A 14-item questionnaire subdivided in two subscales to measure anxiety and depression. Scores for each subscale ranges from 0 (absence of symptoms) to 21 (significant symptoms)

  2. Perceived Stress Scale (PSS-10)

    Time frame: Baseline

    A 10-item questionnaire to measure stress levels related to the perception of unpredicable, uncontrollable, and overloading nature of life. Scores ranges from 0 (low levels) to 40 (high levels).

  3. Multidimensional Assessment of Interoceptive Awareness Version 1

    Time frame: Baseline

    A 32-item questionnaire to measure Interoceptive Awareness. Scores ranges from 0 (low interoceptive awareness) to 160 (high interoceptive awareness).

  4. Body Appreciation Scale-2 (BAS-2)

    Time frame: Baseline

    A 10-item questionnaire to measure appreciation. Scores ranges from 10 (low body appreciation) to 50 (high body appreciation).

  5. Functionality Appreciation Scale (FAS)

    Time frame: Baseline

    A 7-item questionnaire to measure body appreciation. Scores ranges from 0 (low functionality appreciation) to 35 (high functionality appreciation)

  6. Pain Catastrophizing Scale (PCS)

    Time frame: Baseline

    A 13-item questionnaire to measure pain-related catastrophizing. Scores ranges from 0 (low catastrophizing ) to 52 (high catastrophizing).

Sponsors and collaborators

Lead sponsor

Istituti Clinici Scientifici Maugeri SpA

Other

Registry information

Official study title

Functional Physiological, Psychological and Biochemical Reactivity to Social Evaluated Cold Pressor Test in Hereditary Angioedema Patients

Acronym: FROSEN

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
May 16, 2024
Registry last updated
May 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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