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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06100068
Other study ID # EC/2023/0256 (PA-2023-0017)
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 27, 2023
Est. completion date September 1, 2024

Study information

Verified date April 2024
Source University Hospital, Ghent
Contact Liv Veldeman, MD, PhD
Phone +3293323015
Email Liv.Veldeman@uzgent.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In the HOBBIT-trial by Vakaet et al. A protocol was developed to increase breath-hold time using (voluntary) hyperventilation and oxygenation to achieve DIBH times around 3 minutes. Multiple non-medical interventions are being investigated to prolong a L-DIBH that are feasible in clinical practice. One of these methods will be to alter the time perception of the subjects. It has been noted in multiple studies (both medical and not) that slowing a person's perception of time results in an increase in breath-hold time. This alteration in time perception can be achieved with the use of a slowed clock as well as the usage of mental or physical exercises to preoccupy the subjects. Volunteers will then be randomised into either the standard arm or the intervention arm. The intervention arm will follow standard protocol regarding DIBH preparation, though during the L-DIBH they will be asked to perform a simple mental exercise on a tablet. After 2 sessions of 3 L-DIBHs each, there will be a cross-over to the other arm in order to ascertain comfort and preference with each technique.


Description:

Adjuvant radiation therapy has a well-established role in the treatment of breast cancer complementing surgery and systemic treatment, improving survival and local control in both local and regional disease. The long-term follow-up, however, does show increased cardiac morbidity and mortality. The risk of heart disease is greatest in patients receiving a higher heart dosage i.e., left sided breast cancer and irradiation of the internal mammary lymph nodes and does not appear to have a threshold. Lowering heart dose can be achieved by improved planning methods as well as increasing the distance between the target volume and the heart. A deep inspiration breath-hold (DIBH) is often used to this end. An unassisted DIBH is between 12 and 30 seconds; a simple breast irradiation averages 4 DIBHS for completion. More advanced radiotherapy plans (including lymph nodes) needs up to 20 DIBHs. This great amount is both physically and mentally exhausting. A protocol was developed to increase breath-hold time using (voluntary) hyperventilation and oxygenation to achieve DIBH times around 3 minutes. Multiple non-medical interventions are being investigated to prolong a L-DIBH that are feasible in clinical practice. One of these methods will be to alter the time perception of the subjects. It has been noted in multiple studies (both medical and not) that slowing a person's perception of time results in an increase in breath-hold time. This alteration in time perception can be achieved with the use of a slowed clock as well as the usage of mental or physical exercises to preoccupy the subjects. Other important factors on the duration of breath holds are stress and anxiety, which may also be influenced by (relaxation) exercises (including Abdominal breathing). The standard protocol for the first phase will be based on the results of the original HOBBIT trial. 40 Volunteers will be asked to perform 3 L-DIBHs each preceded by 3 minutes of hyperventilation at 16 breaths/min with 40L/min at FiO2 60%. Volunteers will then be randomised into either the standard arm or the intervention arm. The intervention arm will follow standard protocol regarding DIBH preparation, though during the L-DIBH they will be asked to perform a simple mental exercise on a tablet. Data regarding L-DIBH time, side-effects and volunteer reported stress and comfort will be reported. Volunteers in each group will be asked to perform 2 series of 3 L-DIBHs on 2 separate days. After having finished these 2 series, there will be a cross-over to the other arm. This cross-over will evaluate the known effect of the learning bias that we see with breath-hold and show whether this effect has an impact on the anticipated benefit of the intervention. With the cross-over we can also ascertain volunteer comfort and preference with each the technique.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date September 1, 2024
Est. primary completion date July 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Volunteer - Karnofsky index of at least 90 - Able to perform a single DIBH of at least twenty seconds without assistance - Age = 18 years - Informed consent obtained, signed and dated before specific protocol procedures - Female Exclusion Criteria: - Pregnant women - Volunteers above WHO Obesity class II (BMI>35kg/m²) - Subjects on oxygen treatment during day or night - COPD or Asthma patients - Volunteers with pulmonary hypertension - Gastric tube present - Smoking - Previous and substantial breath-holding experience in the past year (e.g., diver, etc.) - Mental condition rendering the volunteer unable to understand the nature, scope and possible consequences of the study

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mental Exercises and Temporal Alteration
Mental exercises during L-DIBH to distort the awareness of passage of time

Locations

Country Name City State
Belgium University Hospital - Radiotherapy Department Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

References & Publications (5)

Darby SC, Ewertz M, McGale P, Bennet AM, Blom-Goldman U, Bronnum D, Correa C, Cutter D, Gagliardi G, Gigante B, Jensen MB, Nisbet A, Peto R, Rahimi K, Taylor C, Hall P. Risk of ischemic heart disease in women after radiotherapy for breast cancer. N Engl J Med. 2013 Mar 14;368(11):987-98. doi: 10.1056/NEJMoa1209825. — View Citation

Early Breast Cancer Trialists' Collaborative Group (EBCTCG); Darby S, McGale P, Correa C, Taylor C, Arriagada R, Clarke M, Cutter D, Davies C, Ewertz M, Godwin J, Gray R, Pierce L, Whelan T, Wang Y, Peto R. Effect of radiotherapy after breast-conserving surgery on 10-year recurrence and 15-year breast cancer death: meta-analysis of individual patient data for 10,801 women in 17 randomised trials. Lancet. 2011 Nov 12;378(9804):1707-16. doi: 10.1016/S0140-6736(11)61629-2. Epub 2011 Oct 19. — View Citation

Schwarz MA, Winkler I, Sedlmeier P. The heart beat does not make us tick: the impacts of heart rate and arousal on time perception. Atten Percept Psychophys. 2013 Jan;75(1):182-93. doi: 10.3758/s13414-012-0387-8. — View Citation

Vakaet V, Van Hulle H, Schoepen M, Van Caelenberg E, Van Greveling A, Holvoet J, Monten C, De Baerdemaeker L, De Neve W, Coppens M, Veldeman L. Prolonging deep inspiration breath-hold time to 3 min during radiotherapy, a simple solution. Clin Transl Radiat Oncol. 2021 Feb 23;28:10-16. doi: 10.1016/j.ctro.2021.02.007. eCollection 2021 May. — View Citation

Vigran HJ, Kapral AG, Tytell ED, Kao MH. Manipulating the perception of time affects voluntary breath-holding duration. Physiol Rep. 2019 Dec;7(23):e14309. doi: 10.14814/phy2.14309. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Breath-Hold related side-effects Various side-effects (regarding, nausea, dizziness, coughing, palpitations, cramps) 1 year
Primary Difference in average L-DIBH time between standard and experimental L-DIBH Difference in average L-DIBH time between standard and experimental L-DIBH 1 year
Secondary Patient reported comfort Comfort on a scale of 0 to 10 where 0 is not comfortable at all and 10 is very comfortable 1 year
Secondary Patient preferece for standard or experimental L-DIBH setup What setup do patients prefer 1 year
Secondary Average L-DIBH time average time of a L-DIBH (in standard and experimental setup) 1 year
Secondary Median L-DIBH time Median time of a L-DIBH (in standard and experimental setup) 1 year
Secondary Minimum and Maximum L-DIBH time Minimum and Maximum time of a L-DIBH (in standard and experimental setup) 1 year
Secondary Oxygen Saturation Oxygen Saturation during the L-DIBH 1 year
Secondary Heart Rate Heart Rate during the hyperventilation and during the L-DIBH 1 year
Secondary Patient report Pain Pain on a scale of 0 to 10 where 0 is no pain and 10 is the worst pain possible 1 year
Secondary Correctness of the mental exercise A grading (perfect-good-fair-poor) regarding the score achieved during the mental exercise 1 year
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