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NCT Number: NCT07730957

Protocolized Receptive Music Intervention to Reduce Care Refusal in Nursing Home Residents With Major Neurocognitive Disorders

The goal of this randomized study is to find out whether using a structured, protocolized music program (MUSIC CARE©) during daily hygiene care can reduce care refusal in older adults with dementia (memory and thinking conditions) who live in nursing homes (EHPADs).

What is "care refusal"? Care refusal (also called resistance to care) happens when a person with dementia refuses or becomes distressed during everyday care activities such as bathing, dressing, or taking medications. It is a very common situation in nursing homes that can be stressful for both residents and care staff.

The main questions this study aims to answer are:

* Can a structured, daily music program reduce care refusal during bathing and hygiene care compared to current practice? * Does using music for 20 minutes during the care session work as well as - or differently from - using it both before and during care (40 minutes total)? * Does the music program also reduce distressing behavioral symptoms in residents? * Does it reduce the need for sedative or psychiatric medications? * Does it reduce professional burnout in caregivers who perform hygiene care?

Researchers will compare three groups:

* Group 1 (Control): Current practice - care staff may use MUSIC CARE© at their own discretion, as they already do * Group 2 (Music During Care): Structured use of MUSIC CARE© for 20 minutes during every hygiene care session, daily for 4 weeks * Group 3 (Music Before + During Care): Structured use of MUSIC CARE© for 20 minutes before and 20 minutes during every hygiene care session (40 minutes total), daily for 4 weeks

Nursing homes (not individual residents) are randomly assigned to a group.

Residents and their caregivers will:

* Have their level of care refusal recorded daily for 4 weeks * Have neuropsychiatric symptoms and medication use assessed at the start, Week 4, and Week 8 * Caregivers will also complete a confidential and anonymous professional burnout questionnaire at 3 time points

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Key information

About this study

  • Background and Rationale

Behavioral and psychological symptoms of dementia (BPSD) are among the most challenging aspects of dementia care, affecting up to 90% of individuals at some point in their disease course. While apathy, anxiety, and depression are the most common BPSD, agitation, aggression, and opposition to care - particularly during direct nursing care activities (bathing, dressing, medication administration) - are frequently reported by both family and professional caregivers.

Care refusal (also termed resistance to care) is defined as any verbal or non-verbal attitude of refusal to accept care, food, hygiene activities, or participation in daily activities. It interferes directly with caregivers' ability to perform activities of daily living assistance, such as bathing, dressing, meal support, and medication administration. It can be misinterpreted as aggression and may lead to inappropriate therapeutic escalation, including physical restraint or psychotropic medication prescription, both of which carry significant adverse effects. In all cases, care refusal should be interpreted as a genuine expression of refusal, even when cognitive autonomy is impaired.

Non-pharmacological interventions (NPIs) are recommended as first-line approaches for BPSD management by French health authorities (HAS) and international expert bodies. Among NPIs, music therapy is one of the best-evidenced techniques, with demonstrated effects on apathy, anxiety, depression, cognitive and emotional competencies, and pain. However, its potential in reducing care refusal specifically has received limited study attention.

  • Rationale for the Intervention

MUSIC CARE© is a validated clinical digital therapy tool (Class 1 Medical Device, CE-marked), developed in France, that uses algorithmically generated personalized music sequences based on the principles of hypnoanalgesia. It follows a standardized "U-sequence" protocol with three phases: an induction phase (stimulating, gradually slowing), a relaxation phase (minimal instrumentation, slow tempo), and a wake phase (gradual return toward initial parameters). Sequences are exclusively composed for MUSIC CARE©, are instrumental, and are free of lyrics to minimize the risk of emotional re-activation through familiar melodies. The tool has a catalogue of 58 sequences across a wide variety of musical styles and can be adapted to individual musical preferences.

MUSIC CARE© has been deployed across LNA Santé establishments since 2021. Clinical observation suggested that while the tool is available, its use in care refusal situations remains inconsistent and practitioner-dependent. Based on scientific literature indicating that psychosocial interventions require structured, protocolized implementation (at least twice weekly, minimum 12 sessions) to demonstrate measurable effects on BPSD, this study was designed to evaluate the impact of formalizing MUSIC CARE© use as a care prescription during hygiene situations.

  • Study Design

OPPOZIC' is a prospective, multicenter, cluster-randomized, open-label study conducted across 15 EHPAD (nursing homes) within the LNA Santé group in France.

Cluster randomization is performed at the EHPAD level: all residents from a given EHPAD are assigned to the same arm (Control, Interventional 1, or Interventional 2). This approach was chosen to ensure feasibility of uniform staff practice within each facility and to enable assessment of protocolization effects at the facility level. Randomization is centralized by LNA Santé before the first resident is enrolled in each facility.

The study involves two populations:

  • Residents: elderly residents with major neurocognitive disorders presenting care refusal during hygiene care (primary population; n=60)
  • Caregivers (soignants): nursing and care staff performing hygiene care for enrolled residents (secondary population; approximately 10-30 per EHPAD, for a total estimated n=150-450) The study is open-label: blinding is not feasible for a behavioral/digital therapeutic intervention.
  • Intervention Description by Arm

Arm A - Control: Standard Care (Current Practice) No change to current facility care practices is required. MUSIC CARE© is available to care staff and may be used at their own clinical judgment and discretion, as is currently practiced in LNA Santé facilities. When a care refusal situation is identified, the resident's medical file is reviewed for potential inclusion. This arm reflects real-world current standard of care and serves as the comparator for the protocolized intervention arms.

Arm B - Interventional 1: Protocolized MUSIC CARE© During Hygiene Care (20 minutes) MUSIC CARE© is protocolized and formally integrated into the resident's personalized care plan (equivalent to a medication prescription). When a care refusal situation is identified, the care team implements a structured MUSIC CARE© intervention during hygiene care. A caregiver enters the resident's room with the MUSIC CARE© tablet and speaker/headphones at the time of care. A 20-minute U-sequence, personalized to the resident's musical preferences, is programmed and played throughout the care session (preparation, hygiene care, installation). This protocol is applied daily for 4 weeks.

Arm C - Interventional 2: Protocolized MUSIC CARE© Before and During Hygiene Care (40 minutes total) The approach is identical to Arm B, with the addition of a 20-minute music session delivered before the hygiene care. The caregiver visits the resident 20 minutes before the care session to start the first U-sequence, then programs a second U-sequence during the care itself. Total daily music intervention: 40 minutes. This protocol is applied daily for 4 weeks.

  • Standard Care Program

All arms continue to receive standard geriatric nursing care within the EHPAD (medical monitoring, nutritional support, social activities, other non-pharmacological approaches as clinically indicated). MUSIC CARE© use in control arm facilities is not prohibited; it is simply not protocolized.

  • Visit Schedule and Procedures

Resident pathway:

  • Pre-selection (Day -7) Eligibility check; information letters provided to resident and/or representative; 7-day reflection period
  • Inclusion / Baseline (Day 0) Written informed consent; demographics; MMSE; NPI-ES (multidisciplinary team); psychotropic medications (last 4 weeks); start of care refusal and duration tracking
  • Weeks 1-4 (S1-S4) - daily Degree of care acceptance/refusal (4-level scale); duration of hygiene care session; adverse event monitoring
  • Follow-up assessment (Week 4 ± 3 days) NPI-ES; psychotropic medications (J0→S4); protocolization data (sessions completed, staff involved)
  • End-of-study assessment (Week 8) NPI-ES; psychotropic medications (S4→S8); adverse events

Caregiver pathway:

  • Pre-selection (Day -7) Information letter provided; 7-day reflection period Inclusion (Day 0) Written informed consent; Maslach Burnout Inventory (MBI) - anonymous
  • Week 4 (S4) Maslach Burnout Inventory (anonymous)
  • Week 8 (S8) Maslach Burnout Inventory (anonymous)
  • Assessment Tools

4-Level Ordinal Care Acceptance/Refusal Scale - Primary Outcome Measure

A structured 4-category observational scale recorded daily by caregivers during hygiene care:

  • Category 1: No refusal - complete care performed without negotiation
  • Category 2: Complete care performed with negotiation
  • Category 3: Partial care performed with negotiation
  • Category 4: Complete refusal or failure (including paradoxical anxiety activation or emotional re-activation triggered by music) Score range: 1 (best) to 4 (worst). Category 4 is treated as complete refusal/failure in all statistical analyses (per CPP recommendation). Lower score = better care acceptance. Assessed daily, Days 1-28.

NPI-ES (Neuropsychiatric Inventory - Nursing Staff version) The NPI-ES is a validated caregiver-report instrument assessing 12 behavioral and neurovegetative domains in patients with dementia: delusions, hallucinations, agitation/aggression, depression/dysphoria, anxiety, euphoria, apathy/indifference, disinhibition, irritability/emotional lability, aberrant motor behavior, sleep, and appetite/eating disorders. Each domain score = Frequency (1-4, or 0 if absent) × Severity (1-3, or 0 if absent). Total behavioral score (10 domains): 0 to 120; higher score = more severe neuropsychiatric symptoms. A caregiver professional burden subscale (0-5 per domain) is assessed separately and is not included in the total score.

Maslach Burnout Inventory (MBI) - Caregiver Outcome

The MBI is a 22-item self-report questionnaire assessing professional burnout, completed anonymously by caregivers. Each item rated on a frequency scale (0 = never to 6 = daily). Three subscales:

  • Emotional Exhaustion (9 items, total 0-54): score <17 = low burnout; 18-29 = -moderate; ≥30 = high. Higher = greater burnout.
  • Depersonalization (5 items, total 0-30): score <5 = low burnout; 6-11 = moderate; ≥12 = high. Higher = greater burnout.
  • Personal Accomplishment (8 items, total 0-48): score ≥40 = low burnout; 34-39 = moderate; ≤33 = high. Higher = LESS burnout (reversed direction for this subscale).

(8) Statistical Analysis Plan Statistical analyses will be performed using R software (v4.3.2 or later) by the LNA Santé Research Support Unit. All tests are two-sided at a global alpha of 5%. p < 0.05 is considered statistically significant. 95% confidence intervals are reported throughout.

  • Descriptive statistics: Continuous variables described as mean ± SD (with normality assessment) and median [Q1-Q3, min-max]. Categorical/discrete variables as n (%).
  • Primary outcome - care acceptance/refusal scale (ordinal, 4 categories):

The primary outcome (score 1-4) may be analyzed as a discrete variable using Pearson's Chi-square or Fisher's exact test. A Poisson regression (or logistic regression focusing on score 4 = refusal/failure) will estimate odds ratios between the three randomization groups. Category 4 (paradoxical reaction/anxiety) is treated as complete refusal/failure in all analyses (per CPP requirement).

  • Between-group comparisons (3 arms): ANOVA or Kruskal-Wallis for continuous variables; Chi-square or Fisher's exact test for categorical variables. Pairwise comparisons: t-test or Mann-Whitney U, Chi-square; no p-value correction given exploratory nature.
  • Temporal evolution (repeated measures at J0, S4, S8): Mixed-effects models with patient/resident as random effect, using the most appropriate regression (linear, logistic, or Poisson). NPI-ES total and subscale scores, Maslach subscale scores, and psychotropic medication use will be analyzed at each time point.
  • Exploratory analyses: Subgroup analyses if sample sizes allow. Multivariate models if confounders are identified.
  • Sample size: 60 residents (4/center × 15 centers) over 18 months. Defined based on inclusion potential, given the exploratory nature of the study. Caregiver participation: estimated 10-30 per EHPAD (total ~150-450).

(9) Benefit/Risk Analysis

Expected benefits for residents: Reduction in care refusal and distress during hygiene care; possible reduction in psychotropic medication use; improved quality of care interactions.

Expected benefits for caregivers: Facilitated hygiene care; improved caregiver-resident relationship; reduced professional burnout; enhanced sense of professional accomplishment.

Expected benefits for LNA Santé: Evidence-based protocol for MUSIC CARE© as a non-pharmacological care prescription; standardized clinical practice.

Identified risks (minimal):

  • Paradoxical anxiety activation or emotional re-activation (triggered by music associated with a past trauma): managed by study exit as per principal investigator decision; treated as complete refusal (score 4) in statistical analyses per CPP requirement.

This study is classified under Loi Jardé, Category 2 (minimal risk and constraints). No ANSM authorization is required.

Who can participate

Healthy volunteers accepted: No

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

RESIDENT ELIGIBILITY

Inclusion criteria

  • Living in a LNA Santé EHPAD (nursing home) as a permanent resident for at least 3 months
  • Diagnosed Alzheimer's disease or a related disorder, or confirmed cognitive decline shown by a Mini-Mental State Examination (MMSE - a short memory and thinking test) score of 24 or less within the past 12 months (including cases where the MMSE cannot be administered due to severe cognitive impairment)
  • Showing care refusal behavior, defined as an Agitation/Aggression item score on the NPI-ES scale (frequency × severity) greater than or equal to 4 at the time of inclusion
  • Resident and/or their legal representative or trusted person has given written consent to participate
  • Affiliated to a French social security scheme

Exclusion criteria

  • Uncompensated hearing loss with sensory isolation (unable to benefit from music therapy)
  • Documented end-of-life status in the medical record

CAREGIVER ELIGIBILITY

Inclusion criteria

(Caregivers):

  • Adult (18 years of age or older)
  • Working in the care unit of an enrolled resident and performing hygiene/nursing care (bathing)
  • Able to read and write French
  • Affiliated to a French social security scheme
  • Has given written consent to participate

Exclusion criteria

(Caregivers):

  • Employment contract shorter than the resident's 3-month study follow-up period (i.e., unable to complete all 3 caregiver assessments)
  • Unable to provide informed consent to participate
  • Under legal protection as defined by Article 1121-8 of the French Public Health Code (under legal guardianship or deprived of liberty)
  • Not affiliated to a French social security scheme

Treatment and study plan

Receptive Music Therapy

Device

MUSIC CARE© is a CE-marked Class 1 Medical Device delivering personalized digital receptive music therapy. Algorithmically composed music sequences follow a standardized "U-sequence" protocol (induction → relaxation → wake phases). Sequences (58 available, 15-90 min) are exclusively instrumental, without lyrics. Personalized to each resident's musical preferences. Delivered via tablet and speaker/headphones. Dosing: 20 min/day during care (Arm 2) or 20 min before + 20 min during care (Arm 3) for 4 weeks.

Other names: Music Care, Receptive Music Intervention, Digital Music Therapy

Standard Nursing Home Care

Other

Standard geriatric nursing care as practiced in LNA Santé EHPAD facilities, including medical monitoring, nursing care, hygiene assistance, nutrition support, social activities, and non-pharmacological approaches as clinically indicated. In the control arm, MUSIC CARE© may be used at caregiver discretion (current standard practice) but is not protocolized.

Primary outcomes

  1. Daily Degree of Hygiene Care Acceptance or Refusal as Assessed by a 4-Level Ordinal Scale Over 4 Weeks

    Time frame: Daily from Day 1 to Day 28 (Weeks 1-4)

    A 4-category ordinal scale recorded daily by caregivers: 1 = No refusal (complete care without negotiation); 2 = Complete care with negotiation; 3 = Partial care with negotiation; 4 = Complete refusal/failure (including paradoxical anxiety or emotional re-activation triggered by music). Score range: 1 to 4; lower score = better care acceptance. Category 4 is defined as refusal/failure in all analyses

Secondary outcomes

  1. Daily Duration of Hygiene Care Session Over 4 Weeks (Minutes)

    Time frame: Daily from Day 1 to Day 28 (Weeks 1-4)

    Total duration of each hygiene care session recorded daily by caregivers, including negotiation time and care time (preparation, hygiene, installation). Assessed in minutes per session. Lower duration may indicate improved care cooperation or efficiency.

  2. Change from Baseline in Neuropsychiatric Symptoms as Assessed by the Neuropsychiatric Inventory - Nursing Staff Version (NPI-ES) at Week 4

    Time frame: Baseline (Day 0) and Week 4

    The NPI-ES assesses 12 behavioral and neurovegetative domains in dementia patients. Each domain score = Frequency (1-4, or 0 if absent) × Severity (1-3, or 0 if absent). Total behavioral score (10 domains): 0 to 120; higher score = more severe neuropsychiatric symptoms. A professional burden subscale (0-5 per domain) is assessed separately.

  3. Change from Baseline in Neuropsychiatric Symptoms as Assessed by the Neuropsychiatric Inventory - Nursing Staff Version (NPI-ES) at Week 8

    Time frame: Baseline (Day 0) and Week 8

    The NPI-ES assesses 12 behavioral and neurovegetative domains. Total behavioral score (10 domains): 0 to 120; higher score = more severe neuropsychiatric symptoms. Week 8 assessment measures persistence of effect 4 weeks after the end of the protocolized intervention period.

  4. Change from Baseline in Monthly Psychotropic Medication Use at Week 4

    Time frame: 4 weeks prior to Baseline (Day 0) and Weeks 1-4 (J0 to S4)

    Monthly consumption of psychotropic medications (recorded by category: benzodiazepines, antidepressants, neuroleptics, hypnotics) from resident's medical records, both as standing prescriptions and as-needed use. Assessed at Week 4 for the interval J0-S4. Lower use reflects potential reduction in pharmacological management of BPSD.

  5. Change from Baseline in Monthly Psychotropic Medication Use at Week 8

    Time frame: Weeks 5-8 (S4 to S8)

    Monthly psychotropic medication consumption (benzodiazepines, antidepressants, neuroleptics, hypnotics) from resident's medical records, assessed for the period S4 to S8. Evaluates sustained reduction in pharmacological BPSD management after the intervention period.

  6. Change from Baseline in Caregiver Professional Burnout as Assessed by the Maslach Burnout Inventory (MBI) at Week 4

    Time frame: Baseline (Day 0) and Week 4

    The MBI is a 22-item self-report scale, completed anonymously by caregivers. Items rated 0 (never) to 6 (every day). Three subscales: (1) Emotional Exhaustion (9 items): range 0-54; higher = greater burnout; cut-offs: <17 low, 18-29 moderate, ≥30 high; (2) Depersonalization (5 items): range 0-30; higher = greater burnout; cut-offs: <5 low, 6-11 moderate, ≥12 high; (3) Personal Accomplishment (8 items): range 0-48; higher = LESS burnout; cut-offs: ≥40 low, 34-39 moderate, ≤33 high.

  7. Change from Baseline in Caregiver Professional Burnout as Assessed by the Maslach Burnout Inventory (MBI) at Week 8

    Time frame: Baseline (Day 0) and Week 8

    Same MBI instrument as Outcome 7. Week 8 assessment evaluates whether any improvement in caregiver burnout is sustained after the 4-week intervention period. MBI subscale ranges and directions: Emotional Exhaustion 0-54 (higher = worse), Depersonalization 0-30 (higher = worse), Personal Accomplishment 0-48 (higher = better).

  8. Rate of MUSIC CARE© Protocolization as Measured by Number of Caregivers Using the Intervention and Number of Sessions Completed at Week 4

    Time frame: Week 4

    Two measures of protocolization compliance: (1) Number of caregivers (soignants) in the unit who performed MUSIC CARE© sessions during Weeks 1-4; (2) Total number of MUSIC CARE© sessions completed in the unit during Weeks 1-4. Higher rates indicate greater uptake and adoption of the protocolized intervention at the team level.

  9. Rate of MUSIC CARE© Protocolization as Measured by Number of Caregivers Using the Intervention and Number of Sessions Completed at Week 8

    Time frame: Week 8

    Same measures as Outcome 9, assessed at Week 8 (4 weeks after the end of the formal protocolized intervention period). Evaluates whether protocolized music use has been maintained spontaneously in the 4 weeks following the formal study period.

Study contacts

Contact information is provided by the study sponsor or research team.

Eva BRIAND

CONTACT

[email protected]

(0)240160161 ext +33

Sponsors and collaborators

Lead sponsor

LNA SANTE

Other

Registry information

Official study title

Impact of Protocolizing Receptive Music Intervention on Care Refusal During Hygiene Care in Nursing Home Residents With Major Neurocognitive Disorders

Acronym: OPPOZIC'

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jul 28, 2026
Registry last updated
Jul 28, 2026

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

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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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