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Multisensory Interventions Reduce MRI Anxiety in Cancer Patients

Multisensory Therapy Alleviating MRI-Related Anxiety in Cancer Patients Via Brain-Autonomic Network Modulation: A Randomized Clinical Trial

MRI-related anxiety is prevalent among cancer patients and frequently undermines imaging quality by inducing motion artifacts or causing premature examination termination. Safe, non-pharmacological supportive interventions have the potential to alleviate procedural anxiety, yet the underlying neurobiological mechanisms remain unclear. This study aimed to investigate the anxiolytic effect of a combined multisensory intervention integrating music therapy and aromatherapy during MRI procedures, and to further explore its potential neurophysiological mechanisms via autonomic nervous system monitoring and resting-state functional magnetic resonance imaging (rs-fMRI).

This study adopted a prospective, single-center, parallel-group randomized controlled trial design and was conducted at Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, between April 2025 and April 2026. Eligible participants were randomly allocated to four groups in equal proportions to receive routine care, music therapy alone, aromatherapy alone, or combined music and aromatherapy interventions. All study interventions were delivered consistently throughout the pre-MRI waiting period and the formal MRI scanning procedure, while participants in the control group received only standard clinical care without additional supportive intervention.

Przegląd badań

Szczegółowy opis

Cancer patients frequently experience significant anxiety during MRI examinations. The confined scanning environment, persistent acoustic noise, and mandatory prolonged immobilization inherent to MRI protocols collectively induce intense procedural stress. Such anxiety commonly causes motion artifacts, impairs diagnostic image quality, and may lead to premature scan termination. Beyond compromising imaging efficiency and accuracy, MRI-triggered psychological distress aggravates the overall psychological burden of cancer patients and may perturb systemic neuroendocrine and immune homeostasis, potentially affecting long-term disease prognosis.

Procedural anxiety arises from dynamic crosstalk between central neural circuits and peripheral autonomic regulatory systems. Chronic stress in oncological populations hyperactivates sympathetic tone and the hypothalamic-pituitary-adrenal axis, driving neuroendocrine dysfunction and immunosuppression. Multiple core brain networks, including the default mode, salience, and executive control networks, govern anxiety processing, with disrupted functional connectivity closely linked to anxiety severity. Concurrent HRV and neuroimaging research further confirms that acute MRI stress distorts bidirectional communication between cortical emotional regulatory regions and subcortical autonomic control centers.

Complementary interventions have emerged as safe, scalable strategies for mitigating cancer-related psychological distress. The 2023 joint clinical guidelines from the Society for Integrative Oncology and the American Society of Clinical Oncology endorse music therapy and aromatherapy for relieving cancer-associated anxiety. Each modality exerts independent anxiolytic effects via distinct neural and physiological pathways. Preliminary clinical evidence suggests that combined auditory and olfactory multisensory interventions may yield superior anxiolytic outcomes compared with single-modality approaches during stressful medical procedures.

Current literature lacks systematic evidence regarding the synergistic neurobiological mechanisms of combined music and aromatherapy for MRI-specific anxiety in cancer patients. Existing studies predominantly rely on subjective psychological assessments without synchronized objective autonomic and brain network profiling. This prospective randomized controlled trial addresses these research gaps by adopting a multi-dimensional evaluation system to characterize the behavioral, physiological, and neural effects of integrated multisensory intervention, aiming to provide mechanistic evidence for standardized supportive care protocols in oncological imaging practice.

This prospective, single-center, four-arm parallel-group randomized controlled trial was conducted at Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, from April 2025 to April 2026. The study protocol was ethically approved (SKSY-2024-480-03), implemented in strict accordance with the Declaration of Helsinki and CONSORT 2025 guidelines, and pre-registered in the National Medical Research Registration and Information System of China (MR-44-25-034307). All participants provided written informed consent prior to enrollment.

This study enrolled eligible adult oncology patients requiring routine clinical MRI examinations, with unified enrollment specifications formulated to ensure homogeneous study populations.

Standardized exclusion criteria were established to exclude populations that might compromise intervention safety, data authenticity and research credibility.

Eligible participants were equally randomized into four parallel groups (1:1:1:1 allocation): routine care control, single music therapy, single aromatherapy, and combined multisensory intervention. Randomization was performed via computer-generated random numbers with sealed opaque envelopes by an independent researcher blinded to recruitment, intervention delivery, and outcome evaluation.

Due to the sensory nature of the interventions, participant blinding was not achievable. However, all data analysts, neuroimaging processors, and clinical radiologists remained fully blinded to group allocation throughout the trial to minimize detection bias.

All intervention protocols were initiated during the pre-scan waiting phase and sustained continuously throughout the entire MRI scanning procedure.

Control Group: Participants received standard clinical MRI care and routine pre-scan guidance without additional supportive interventions, with continuous vital sign monitoring throughout the procedure.

Music Therapy Group: Based on standard care, participants received standardized pre-scan autonomic monitoring followed by continuous exposure to a validated soothing traditional Chinese pentatonic guzheng musical stimulus via MRI-compatible headphones throughout scanning.

Aromatherapy Group: With consistent pre-scan autonomic monitoring, participants received standardized lavender olfactory stimulation via a fixed collar absorbent pad during the entire MRI procedure, with natural breathing maintained throughout.

Combined MT + AT Group: Participants received synchronized music and aromatherapy multisensory stimulation, with both interventions initiated after baseline physiological stabilization and sustained across the full scanning process.

The selected musical stimulus features high melodic consonance and smooth pentatonic structure to avoid triggering physiological alert responses. Lavender essential oil was selected based on robust meta-analytic evidence for reliable anxiolytic efficacy, with its core volatile components modulating central nervous system activity via olfactory transduction pathways.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

152

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Guangdong
      • Guangzhou, Guangdong, Chiny, 510120
        • Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Aged 18 to 60 years
  • Pathologically confirmed malignant tumor
  • Require clinically indicated MRI examination
  • Baseline HADS anxiety subscale score ≥ 8
  • Able to understand study procedures and provide written informed consent

Exclusion Criteria:

  • Severe cognitive impairment or preexisting neurological disorders that compromise neuroimaging data quality
  • Confirmed olfactory or auditory dysfunction
  • Known hypersensitivity to aromatic essential oils
  • MRI contraindications (implanted metallic devices, severe claustrophobia) or unstable cardiovascular conditions
  • Concurrent enrollment in other interventional clinical trials

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie podtrzymujące
  • Przydział: Randomizowane
  • Model interwencyjny: Przypisanie czynnikowe
  • Maskowanie: Pojedynczy

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Brak interwencji: Control Group (Routine imaging care only)
Patients receive standard routine imaging care without any additional music or aromatherapy interventions. Standard vital sign monitoring is conducted for 20 minutes before MRI and maintained throughout the whole scan procedure.
Eksperymentalny: MT Group (Guzheng music intervention)
On the basis of routine imaging care, patients receive 20 minutes of autonomic monitoring before MRI. After 10 minutes of baseline monitoring, participants listen to the guzheng piece Fishing Boat Singing at Dusk via MRI-compatible headphones; autonomic monitoring continues until scan completion.
Patients listen to the traditional Chinese guzheng piece Fishing Boat Singing at Dusk via MRI-compatible noise-isolating headphones continuously during MRI scanning. The music intervention starts after 10 minutes of baseline autonomic monitoring within the 20-minute pre-examination monitoring window.
Eksperymentalny: AT Group (Lavender aromatherapy intervention)
Patients complete 20 minutes of autonomic monitoring prior to MRI examination. After 10 minutes of baseline monitoring, 2 drops of Lavandula angustifolia essential oil are applied to an absorbent pad fixed on the patient's collar. Subjects breathe normally, and autonomic monitoring lasts through the entire MRI scan.
Two drops of pure Lavandula angustifolia essential oil are dripped onto an absorbent pad fixed to the patient's collar near the neck before MRI. Patients breathe normally to receive sustained lavender aroma stimulation throughout the entire scan, initiated after 10 minutes of baseline autonomic monitoring.
Eksperymentalny: Combined MT+AT Group (Music plus aromatherapy)
Patients receive both interventions simultaneously during 20-minute pre-MRI autonomic monitoring. Two drops of lavender essential oil are placed on the collar pad, while participants listen to the guzheng piece via MRI-safe headphones. Both sensory stimuli and autonomic monitoring persist for the full duration of MRI scanning.
Patients listen to the traditional Chinese guzheng piece Fishing Boat Singing at Dusk via MRI-compatible noise-isolating headphones continuously during MRI scanning. The music intervention starts after 10 minutes of baseline autonomic monitoring within the 20-minute pre-examination monitoring window.
Two drops of pure Lavandula angustifolia essential oil are dripped onto an absorbent pad fixed to the patient's collar near the neck before MRI. Patients breathe normally to receive sustained lavender aroma stimulation throughout the entire scan, initiated after 10 minutes of baseline autonomic monitoring.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Change in Hospital Anxiety and Depression Scale anxiety subscale score
Ramy czasowe: Baseline (pre-MRI) and within 30 minutes immediately after completion of MRI examination
Difference in anxiety severity quantified using the full Hospital Anxiety and Depression Scale (HADS) anxiety subscale. The subscale ranges from 0 (minimum, no anxiety symptoms) to 21 (maximum, severe anxiety); higher scores correspond to worse anxiety status. Anxiety scores are captured at two distinct time points to compute the pre-to-post MRI score change.
Baseline (pre-MRI) and within 30 minutes immediately after completion of MRI examination

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Change in low-frequency heart rate variability parameter
Ramy czasowe: Baseline (pre-MRI), during MRI scanning, and within 30 minutes immediately after completion of MRI examination
Heart rate variability low-frequency (LF) index derived from continuous 3-lead electrocardiography signals, which quantifies sympathetic nervous system activity. Delta LF values calculated relative to pre-MRI baseline will be compared between study groups.
Baseline (pre-MRI), during MRI scanning, and within 30 minutes immediately after completion of MRI examination
Change in high-frequency heart rate variability parameter
Ramy czasowe: Baseline (pre-MRI), during MRI scanning, and within 30 minutes immediately after completion of MRI examination
Heart rate variability high-frequency (HF) index derived from continuous 3-lead electrocardiography signals, which quantifies parasympathetic nervous system activity. Delta HF values calculated relative to pre-MRI baseline will be compared between study groups.
Baseline (pre-MRI), during MRI scanning, and within 30 minutes immediately after completion of MRI examination
Standardized amplitude of low-frequency fluctuations from resting-state functional MRI
Ramy czasowe: Within 30 minutes after completion of clinical MRI scan and assigned study intervention
Whole-brain standardized amplitude of low-frequency fluctuations (zALFF) derived from 10-minute rs-fMRI. Uniform preprocessing pipelines are applied to compute this metric for intergroup comparison of spontaneous regional brain neural activity.
Within 30 minutes after completion of clinical MRI scan and assigned study intervention
Standardized z-score degree centrality from resting-state functional MRI
Ramy czasowe: Within 30 minutes after completion of clinical MRI scan and assigned study intervention
Whole-brain standardized z-score degree centrality (szDC) derived from 10-minute rs-fMRI. Uniform preprocessing pipelines are applied to compute this metric for intergroup comparison of whole-brain functional connectivity strength.
Within 30 minutes after completion of clinical MRI scan and assigned study intervention

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Publikacje ogólne

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

10 kwietnia 2025

Zakończenie podstawowe (Rzeczywisty)

9 kwietnia 2026

Ukończenie studiów (Rzeczywisty)

10 kwietnia 2026

Daty rejestracji na studia

Pierwszy przesłany

28 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

2 lipca 2026

Pierwszy wysłany (Rzeczywisty)

9 lipca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 lipca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

2 lipca 2026

Ostatnia weryfikacja

1 kwietnia 2025

Więcej informacji

Terminy związane z tym badaniem

Dodatkowe istotne warunki MeSH

Inne numery identyfikacyjne badania

  • SKSY-2024-480-03

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Opis planu IPD

Individual participant data (IPD) will not be shared externally to protect participants' privacy and comply with institutional ethical review board requirements. Raw MRI, HRV and questionnaire records contain identifiable sensitive clinical information, and relevant local privacy regulations prohibit the public release of individual-level raw data.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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