search
Back to results

HOBBIT 3: Mental Exercises and Temporal Alteration (HOBBIT-META)

Primary Purpose

Breast Neoplasm, Radiotherapy, Breath Holding

Status
Not yet recruiting
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Mental Exercises and Temporal Alteration
Sponsored by
University Hospital, Ghent
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Neoplasm

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • University Hospital - Radiotherapy Department

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard L-DIBH

Intervention L-DIBH

Arm Description

Starts with 2 sessions of normal L-DIBH followed by 2 sessions of L-DIBH combined with mental exercises.

Starts with 2 sessions of of L-DIBH combined with mental exercises followed by 2 sessions of normal L-DIBH.

Outcomes

Primary Outcome Measures

Difference in average L-DIBH time between standard and experimental L-DIBH
Difference in average L-DIBH time between standard and experimental L-DIBH

Secondary Outcome Measures

Patient reported comfort
Comfort on a scale of 0 to 10 where 0 is not comfortable at all and 10 is very comfortable
Patient preferece for standard or experimental L-DIBH setup
What setup do patients prefer
Average L-DIBH time
average time of a L-DIBH (in standard and experimental setup)
Median L-DIBH time
Median time of a L-DIBH (in standard and experimental setup)
Minimum and Maximum L-DIBH time
Minimum and Maximum time of a L-DIBH (in standard and experimental setup)
Oxygen Saturation
Oxygen Saturation during the L-DIBH
Heart Rate
Heart Rate during the hyperventilation and during the L-DIBH
Patient report Pain
Pain on a scale of 0 to 10 where 0 is no pain and 10 is the worst pain possible
Correctness of the mental exercise
A grading (perfect-good-fair-poor) regarding the score achieved during the mental exercise

Full Information

First Posted
October 3, 2023
Last Updated
October 20, 2023
Sponsor
University Hospital, Ghent
search

1. Study Identification

Unique Protocol Identification Number
NCT06100068
Brief Title
HOBBIT 3: Mental Exercises and Temporal Alteration
Acronym
HOBBIT-META
Official Title
Hyperventilation and Oxygenation to Increase Breath Hold in Breast Cancer Irradiation Treatment (HOBBIT) 3: Mental Exercises and Temporal Alteration
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 2, 2023 (Anticipated)
Primary Completion Date
April 1, 2024 (Anticipated)
Study Completion Date
September 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Ghent

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasm, Radiotherapy, Breath Holding, Mental Test

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard L-DIBH
Arm Type
Active Comparator
Arm Description
Starts with 2 sessions of normal L-DIBH followed by 2 sessions of L-DIBH combined with mental exercises.
Arm Title
Intervention L-DIBH
Arm Type
Experimental
Arm Description
Starts with 2 sessions of of L-DIBH combined with mental exercises followed by 2 sessions of normal L-DIBH.
Intervention Type
Behavioral
Intervention Name(s)
Mental Exercises and Temporal Alteration
Intervention Description
Mental exercises during L-DIBH to distort the awareness of passage of time
Primary Outcome Measure Information:
Title
Difference in average L-DIBH time between standard and experimental L-DIBH
Description
Difference in average L-DIBH time between standard and experimental L-DIBH
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Patient reported comfort
Description
Comfort on a scale of 0 to 10 where 0 is not comfortable at all and 10 is very comfortable
Time Frame
1 year
Title
Patient preferece for standard or experimental L-DIBH setup
Description
What setup do patients prefer
Time Frame
1 year
Title
Average L-DIBH time
Description
average time of a L-DIBH (in standard and experimental setup)
Time Frame
1 year
Title
Median L-DIBH time
Description
Median time of a L-DIBH (in standard and experimental setup)
Time Frame
1 year
Title
Minimum and Maximum L-DIBH time
Description
Minimum and Maximum time of a L-DIBH (in standard and experimental setup)
Time Frame
1 year
Title
Oxygen Saturation
Description
Oxygen Saturation during the L-DIBH
Time Frame
1 year
Title
Heart Rate
Description
Heart Rate during the hyperventilation and during the L-DIBH
Time Frame
1 year
Title
Patient report Pain
Description
Pain on a scale of 0 to 10 where 0 is no pain and 10 is the worst pain possible
Time Frame
1 year
Title
Correctness of the mental exercise
Description
A grading (perfect-good-fair-poor) regarding the score achieved during the mental exercise
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Breath-Hold related side-effects
Description
Various side-effects (regarding, nausea, dizziness, coughing, palpitations, cramps)
Time Frame
1 year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liv Veldeman, MD, PhD
Phone
+3293323015
Email
Liv.Veldeman@uzgent.be
First Name & Middle Initial & Last Name or Official Title & Degree
Vincent Huybrechts, MD
Email
vincent.huybrechts@uzgent.be
Facility Information:
Facility Name
University Hospital - Radiotherapy Department
City
Ghent
ZIP/Postal Code
9000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22019144
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.
Results Reference
background
PubMed Identifier
23484825
Citation
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.
Results Reference
background
PubMed Identifier
33732910
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.
Results Reference
background
PubMed Identifier
23143915
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.
Results Reference
background
PubMed Identifier
31833235
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.
Results Reference
background

Learn more about this trial

HOBBIT 3: Mental Exercises and Temporal Alteration

We'll reach out to this number within 24 hrs