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DementiaOPPOZIC'NCT07730957

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

A study testing Receptive music therapy and Standard Nursing Home Care in people with Dementia and Cognitive Dysfunction, run by LNA SANTE at 12 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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). Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Receptive music therapy and Standard Nursing Home Care
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
12 sitesFrance
Study dates
30 Oct 2025to 30 Jun 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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
  • Adult (18 years of age or older)
Show all 10Show fewer
  • 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

Who cannot join

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

Trial locations and contacts

12 sites in 1 country. Contact the study team or a site near you to ask about taking part.

12 sites in 1 country

France12 sites, 12 recruiting
  • Les Jardins d'Henriville

    Amiens, 80000

    Claire MARTEIN, DR, (+33)3 60 24 88 00, medec.jardinshenriville@lna-sante.com

    Claire MARTEIN, DR

    Recruiting
  • Villa d'Épidaure Garches

    Garches, 92380

    Merryl ZERBIB, DR, (+33)1 47 01 30 60, merryl.zerbib@lna-sante.com

    Merryl ZERBIB, DR

    Recruiting
  • Villa d'Épidaure La Celle St Cloud

    La Celle-Saint-Cloud, 78170

    Anne JURET, DR, (+33)1 30 78 44 00, ajuret.epidaure78@lna-sante.com

    Anne JURET, DR

    Not yet recruiting
  • La Meulière de la Marne

    La Ferté-sous-Jouarre, 77260

    Sylvie DELALANDE, DR, (+33)1 78 71 12 12, sdelalande.meuliere@lna-sante.com

    Sylvie DELALANDE, DR

    Not yet recruiting
  • Résidence La Chézalière

    Nantes, 44100

    Marie-Anne MAITRE, DR, (+33)2 51 84 78 47, medec.chezaliere@lna-sante.com

    Marie-Anne MAITRE, DR

    Recruiting
  • Parc de Diane

    Nantes, 44200

    Christian BLONZ, DR, (+33)2 51 79 52 00, medec.diane@lna-sante.com

    Christian BLONZ, DR

    Recruiting
  • Résidence Les Nymphéas

    Pacé, 35740

    Nolwenn DELARUE, DR, (+33)2 99 29 63 63, medec.nympheas@lna-sante.com

    Nolwenn DELARUE, DR

    Recruiting
  • Villa Bourgailh

    Pessac, 33600

    Béatrice FONTAINE-MARTINEZ, DR, (+33)5 57 01 94 00, medec.villabourgailh@lna-sante.com

    Béatrice FONTAINE MARTINEZ, DR

    Recruiting
  • Villa Amélie

    Saint-Rogatien, 17220

    Marion CHARENTON, DR, (+33)5 17 83 40 40, medec1.amelie@lna-sante.com

    Marion CHARENTON, DR

    Not yet recruiting
  • Résidence Verte Prairie

    Salon-de-Provence, 13300

    Sylvie DE BESOMBES, DR, (+33)4 90 56 38 00, sdebesombes.verteprairie@lna-sante.com

    Sylvie DE BESOMBES, DR

    Not yet recruiting
  • Villa Tohannic

    Vannes, 56000

    Sophie DREVILLON, DR, (+33)2 56 63 01 00, medec.villatohannic@lna-sante.com

    Sophie DREVILLON, DR

    Not yet recruiting
  • Les Jardins de Leysotte

    Villenave-d'Ornon, 33140

    Isabelle MARCET, DR, (+33)5 64 12 08 00, medec.leysotte@lna-sante.com

    Isabelle MARCET, DR

    Not yet recruiting

Other trials in France

About this study

Official title: Impact of Protocolizing Receptive Music Intervention on Care Refusal During Hygiene Care 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.

Read more

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
Read the detailed description
  1. 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.
  2. 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.
  3. 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.
  1. 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.
  2. 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.
  3. 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)
  1. 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.

Being tested
Receptive music therapy, Standard Nursing Home Care
Keywords
Dementia, Music Therapy, Care Refusal, Receptive Music Intervention, Non-Pharmacological Intervention, Behavioral and Psychological Symptoms of Dementia, Nursing Home, Professional Burnout
Medical subject headings
Dementia, Cognitive Dysfunction, Psychomotor Agitation, Burnout, Professional, Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Receptive music therapyDevice

    Also called Music Care, Receptive Music Intervention, Digital Music Therapy

    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.

  • Standard Nursing Home CareOther

    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.

Study groups in NCT07730957
Study groupRoleWhat they receive
Control: Standard Care (Current Practice)Active comparatorNo change to current facility care practices. MUSIC CARE©, a validated digital therapeutic tool, is available to care staff and may be used at their own discretion as per current standard practice. When a care refusal situation is identified, the resident's medical record is reviewed for potential inclusion. This arm reflects real-world standard of care in LNA Santé EHPAD facilities and serves as the comparator for protocolized intervention arms.
Receives: Other: Standard Nursing Home Care
Interventional 1: MUSIC CARE© During Care (20 minutes/day)ExperimentalMUSIC CARE© is protocolized and prescribed in the resident's personalized care plan. A caregiver enters the resident's room with the MUSIC CARE© tablet and speaker/headphones at the time of hygiene care and programs a 20-minute personalized U-sequence throughout the care session (preparation, hygiene, installation). Music is personalized to the resident's musical preferences. Delivered daily for 4 weeks (maximum 28 sessions).
Receives: Device: Receptive music therapy
Interventional 2: MUSIC CARE© Before and During Care (40 minutes/day)ExperimentalIdentical approach to Arm 2, with an additional 20-minute MUSIC CARE© session immediately before hygiene care. Caregiver visits the resident 20 minutes before care to start the first U-sequence, then programs a second U-sequence during the care session. Total: 40 minutes of protocolized music therapy per day. Delivered daily for 4 weeks (maximum 56 music sessions).
Receives: Device: Receptive music therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

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

    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

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

Secondary outcomes (9)
  1. Daily Duration of Hygiene Care Session Over 4 Weeks (Minutes)

    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.

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

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

    Measured: Baseline (Day 0) and Week 4

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

    Measured: Baseline (Day 0) and Week 8

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

    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.

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

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

    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.

    Measured: Weeks 5-8 (S4 to S8)

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

    Measured: Baseline (Day 0) and Week 4

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

    Measured: Baseline (Day 0) and Week 8

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

    Measured: Week 4

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

    Measured: Week 8

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Jul 2026
  2. Study start30 Oct 2025
  3. Primary completion30 Jun 2027 (estimated)
  4. Study completion30 Jun 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
A multicenter, prospective, cluster-randomized study
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07730957
Sponsor's protocol ID
2024-A00522-45
Acronym
OPPOZIC'
Status last verified
Jul 2026
First submitted
23 Jul 2026
Last updated
28 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Individual participant data (IPD) sharing has not yet been determined. This is a pilot multicenter study (n=60 residents). Data are processed under French GDPR reference methodology MR-001. Caregiver data are fully anonymized. Results will be reported in an internal LNA Santé report and may be submitted for publication in a specialty medical journal. A decision on IPD sharing will be made prior to study completion.

Questions about this trial

What is this clinical trial studying?

A study testing Receptive music therapy and Standard Nursing Home Care in people with Dementia and Cognitive Dysfunction, run by LNA SANTE at 12 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 28 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 12 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Eva BRIAND ((0)240160161 ext +33, eva.briand@lna-sante.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jul 2026.

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