Effectiveness of Flash Mediation Therapy

Dementia Clinical Trial

Official title:

Study on Effectiveness of Flash Mediation Therapy in the Context of Acute Psychological and Behavioral Symptoms of Dementia in Nursing Homes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02933177
• Other study ID #: 69HCL16_0442
• Status: Completed
• Phase: N/A
• First received: October 12, 2016
• Last updated: November 29, 2017
• Start date: May 2016
• Est. completion date: March 2017

Study information

• Verified date: August 2017
• Source: Hospices Civils de Lyon
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In order to offer a non-drug intervention for caregivers in nursing home to respond promptly to a behavioral crisis with an appropriate response to each patient, a chariot has been developed by the Institute of Ageing Well Korian (Institut du Bien Vieillir Korian) to bring together eleven mediation activities. These activities lasting about 15 minutes are based on emotion (reminiscent, games) and sensory interventions (music, massage, touch) to decentralize patient stimulus that disturbs and focus on a subject not disruptive. This emergency intervention should provide a reduction in Behavioral and Psychological Symptom of Dementia (BPSD) of nursing home patients. The main objective is to measure its immediate effect on productive symptoms (agitation, aberrant motor behavior and disinhibition). The secondary objectives are to measure its immediate impact on the well-being and psychotropic treatments, and measure its effect after two months and after four months on all BPSD with a focus on agitation, the administration of psychotropic drugs, the hospitalizations and the number of falls.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 241
• Est. completion date: March 2017
• Est. primary completion date: March 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• People ability to object and does not oppose either by themselves or through a trusted person referred to in Article L. 1111-6 of the Code of Public Health, failing thereof, by the family, or, if a person talking to the person close and stable ties. For adults under guardianship, permission must be given by the legal representative of the person. The research will benefit from the backing of Persons Protection Committee (PPC) prior to its implementation;

• Man or woman over 60 years;

• patient living in one of the nursing homes participating in the project;

• Patient completing the diagnostic criteria for major neurocognitive disorder according to Diagnostic and Statistical Manual of Mental Disorders V criteria (DSM-V)

• The patient must have at least one of these productive symptoms (agitation, aberrant motor behavior, disinhibition) listed by the NPI-NH (score> 2 at least one of these items)

Exclusion Criteria:

• Deafness or blindness may compromise patient assessment or participation in the intervention

Related Conditions & MeSH terms

• Dementia

Intervention

Behavioral:
• 2 months control condition - 4 months chariot-flash
The control condition is to propose the usual procedures for the management of productive symptoms during the emergence or increase of these symptoms. The "chariot-flash" condition is a chariot with eleven drawers. Each drawer contains an activity (lasting about 15 minutes): Boards of known photographs to recall autobiographical memories Newspapers to read, talk, associate memories around an article Massage Oil, refreshing wipes, cream to reconnect with the body Clay, cookie pieces, washable felt and paper to create shapes, draw. Walk with a person of the healthcare team the case of behavioral disorders in type of ambulation and untimely exit . Listening to music Relaxation-Breathing Cushion, foam balls to vent his energy on secure hardware. Plush doll or to invest a vector object of affection and empathy Sensory flash balls that the patient can squeeze, throw, roll. Games with which the patient can play according to its possibilities.
• 4 months control condition-2 months chariot flash
The control condition is to propose the usual procedures for the management of productive symptoms during the emergence or increase of these symptoms. The "chariot-flash" condition is a chariot with eleven drawers. Each drawer contains an activity (lasting about 15 minutes): Boards of known photographs to recall autobiographical memories Newspapers to read, talk, associate memories around an article Massage Oil, refreshing wipes, cream to reconnect with the body Clay, cookie pieces, washable felt and paper to create shapes, draw. Walk with a person of the healthcare team the case of behavioral disorders in type of ambulation and untimely exit . Listening to music Relaxation-Breathing Cushion, foam balls to vent his energy on secure hardware. Plush doll or to invest a vector object of affection and empathy Sensory flash balls that the patient can squeeze, throw, roll. Games with which the patient can play according to its possibilities.

Locations

Country	Name	City	State
France	Hôpital des Charpennes Centre de Recherche Clinique "Vieillissement-Cerveau-Fragilité"	Lyon

Sponsors (1)

Lead Sponsor	Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in number of disorders	the number of disorders are evaluated with Cohen Mansfield Agitation Inventory (CMAI) before and 30 minutes after each intervention.; The original version of the CMAI is initially planned to study the frequency of these disorders. However, the goal being to study the decrease in productive symptoms, after using the "chariot-flash", only the number of this item will be considered (between 0 and 29). For example in this modified version, for the item "pace, aimless wandering" nursing team can answer "present" or "absent" instead of (never, less than once a week, once or twice per week, a few times over week, one to two times daily, several times a day, several times per hour)	until 4 months
Secondary	Change in score of well-being	the score of well-being is assessed using the Instant Well-Being scale (Evaluation Instantané du Bien-Etre : EVIBE) before and 30 minutes after each intervention .; The EVIBE is a visual analogue scale for reporting the status of well-being of the patient at a specific time. On a graduated scale from 0 to 5, the caregiver should position a cursor position to the left corresponding to the feeling of well-being the lowest and the right position to the feeling of well-being the highest.	until 4 months
Secondary	change in psychotropic drugs prescribed	The caregiver or doctor will check on a board what are the treatments that have been added or modified (compared to the usual treatment) in response to behavioral disorder	until 4 months
Secondary	change in score of BPSD	the score of BPSD is assessed using the neuropsychiatric inventory nursing home version (NPI-NH).; Each of the 12 BPSD (delusions, hallucinations, agitation, depression, anxiety, excitement, apathy, disinhibition, depression, motor aberrant behavior, sleep and appetite) is evaluated on 12 depending on its frequency and severity (global score =144).	before the beginning of the study, at 2 months, 4 months and 6 months
Secondary	change in level of agitation	the level of agitation is assessed using the original version of CMAI. The CMAI lists 29 agitation and aggressive behaviors by frequency (0: not evaluable 1: never, 2: less than once a week 3 : once or twice per week, 4 : a few times over week, 5: one to two times daily, 6 : several times a day, 7 : several times per hour) to obtain a score ranging from 0-203.	before the beginning of the study, at 2 months, 4 months and 6 months
Secondary	change in the number of administered psychotropic drugs.	The caregiver or doctor will check on a board on which is written all psychotropic treatments that the patient takes and the dosage	before the beginning of the study, at 2 months, 4 months and 6 months
Secondary	The number of hospitalization	The caregiver or doctor will refer in a table the different hospitalizations during the study and their date	at 2 months, 4 months and 6 months
Secondary	The number of fall	The caregiver or doctor will refer in a table the different falls during the study and their date.	at 2 months, 4 months and 6 months