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Clinical Trials/NCT06281145
NCT06281145
Recruiting
Not Applicable

A Study on Therapeutic Potential of Stress-Reducing Intervention in Patients With Solid Tumors

Comenius University1 site in 1 country100 target enrollmentMarch 15, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Comenius University
Enrollment
100
Locations
1
Primary Endpoint
Primary endpoint - executive functions
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this interventional study is to test the heart-rate variability biofeedback intervention (HRV BI) in 2 cohorts of patients. Cohort A will evaluate the effect of the addition of HRV BI in patients with breast cancer treated in the neoadjuvant setting (vs. standard of care alone, SOC) followed by local therapy (surgery +/-radiotherapy). Cohort B will evaluate the effect of the addition of HRV BI in patients with colon cancer after surgery in the adjuvant setting (vs. standard of care alone, SOC).

Detailed Description

This is a prospective, interventional, clinical study with in 2 cohorts. Target of subjects is 50 per cohort and an anticipated total duration of 36 months. Participants will undergo 4 sessions of HRV BI with the trainer where they will learn about the prognostic role of the vagal nerve in cancer and in reducing distress and pain, and how to perform deep paced breathing with the HRV monitoring. They will perform the training daily (3-times, minimum 7 minutes each) at home with the online control for 3 months. Researchers will compare the effect of addition of 3-months training of HRV BI to SOC on inflammation, HRV, quality of life (QoL), cognitive functions, salivary cortisol slopes, sleep quality and treatment outcomes of patients with colorectal and breast cancer.

Registry
clinicaltrials.gov
Start Date
March 15, 2024
End Date
March 15, 2029
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Comenius University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients older than 18 years.
  • Pathologically confirmed breast cancer indicated for neoadjuvant systemic treatment or colon cancer after curative surgery indicated for adjuvant systemic treatment.
  • Adequate renal functions: measured or calculated (by Cockcroft formula) creatinine clearance \> 60 ml/min.
  • Absolute granulocytes count ≥ 1,500/mm3, platelets ≥ 100,000 mm3, bilirubin ≤ 1.5x the upper limit of normal value.
  • Adequate liver functions defined by AST (Aspartate aminotransferase) and ALT (Alanine transaminase) ≤ 3xUNL (upper normal of limit).
  • Basic computer skills of patient or his family member.
  • Signed informed consent.

Exclusion Criteria

  • Previous chemotherapy.
  • Previous malignancy, except for basal-cell carcinoma of the skin within last 5 years.
  • Patients with know primary immunodeficiency and patients infected by the Human Immunodeficiency Virus (HIV).
  • Patient receiving long term corticosteroid treatment, anti-arrhythmic drugs and opioids who can not withdraw the treatment for the period of application of the heart rate variability (HRV) biofeedback training.
  • Patients with diabetes mellitus, cardiac arrhythmia, cardiac pacemaker implant.
  • Patients who do not fit inclusion criteria.

Outcomes

Primary Outcomes

Primary endpoint - executive functions

Time Frame: 36 months

Effect of HRV biofeedback training on executive functions (HRV biofeedback + SOC, vs. SOC alone) measured by Stroop task mean response time for color-word condition.

Primary endpoint - Working memory

Time Frame: 36 months

The effect of 3-month heart rate variability (HRV) biofeedback training and conventional cancer treatment (standard of care, SOC) vs. SOC alone on working memory measured by digit span test score (the number of remembered digits in the longest passed sequence), for both forward and backward condition.

Primary endpoint - QoL

Time Frame: 36 months

Effect of HRV biofeedback training on quality of life (HRV biofeedback + SOC, vs. The effect of 3-month heart rate variability (HRV) biofeedback training and conventional cancer treatment (standard of care, SOC) vs. SOC alone on EORTC-QLQ-C30 (version 3) score (QLQ- Quality Life Questionnaire). The EORTC-QLQ-C30 has 30 items divided into five functional scales (physical, role, cognitive, emotional, and social), and three symptom scales (fatigue, pain, and nausea and vomiting). The score for each scale as well as the sum score for the whole instrument is standardized to values 0 to 100, with a higher score meaning a worse outcome.

Primary endpoint - inflammation

Time Frame: 36 months

he effect of 3-month heart rate variability (HRV) biofeedback training and conventional cancer treatment (standard of care, SOC) vs. SOC alone on inflammation (IL-6, Tumor necrosis factor α, IL-10 from peripheral blood sample in pg/ml and tumour infiltrating lymphocytes (TIL) in %).

Primary endpoint- salivary cortisol slopes

Time Frame: 36 months

The effect of 3-month heart rate variability (HRV) biofeedback training and conventional cancer treatment (standard of care, SOC) vs. SOC alone on salivary cortisol slopes (difference between bedtime and awakening saliva cortisol concentration in ng/ml).

Primary endpoint- sleep quality

Time Frame: 36 months

The effect of 3-month heart rate variability (HRV) biofeedback training and conventional cancer treatment (standard of care, SOC) vs. SOC alone on sleep quality measured by both actigraphy and self-report data. The main variables are total time spent sleeping (in hours and minutes), and sleep efficiency (proportion of time spent sleeping vs. time spent in bed trying to sleep).

Primary endpoint - heart rate variability (HRV)

Time Frame: 36 months

Effect of HRV biofeedback training on HRV indexed by the root mean square of successive differences between heartbeats (RMSSD) in ms.

Secondary Outcomes

  • Secondary endpoint - Pathologic Complete Response (pCR) and Residual Cancer Burden (RCB) rate in cohort A(36 months)
  • Secondary endpoint - Relapse-free Survival (RFS)(60 months)
  • Secondary endpoint - Overall survival (OS)(96 months)
  • Secondary endpoint - Serious Adverse Events (SAE)(36 months)

Study Sites (1)

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