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Pilot Study of a Robot-assisted Intervention for the Management of Care-induced Pain in Dementia (PARODOL)

Primary Purpose

Moderate to Severe Dementia

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
A : Systemic evaluation of the pain and mediation with the PARO therapeutic robot
B : Systemic evaluation of the pain
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Moderate to Severe Dementia focused on measuring Dementia, Pain, Nursing care, Psychosocial intervention, Robot-assisted therapy, paro robot

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient over 60 years of age
  • Consent to participate
  • Patient diagnosed by a geriatrician or a neurologist with moderate to severe dementia (MMSE<24), according to the criteria of the Diagnostic and Statistical Manual DSM IV-TR (APA,2004) and NINCDS-ADRDA(McKhann et al.1984).
  • Patient living in a nursing home or a long stay department
  • Painful patient during nursing care (pain drugs prescription or direct observation)

Exclusion Criteria:

  • Patient (or patient's legal representative) does not provide consent
  • The presence of acute organic disease or psychiatric decompensation and major neuropsychiatric symptoms incompatible with the intervention.
  • Patient who cannot interact physically with Paro
  • The presence of multidrug-resistant bacteria in patient to reduce the risk of contamination.

Sites / Locations

  • Résidence Mutualiste " L'adret "
  • Résidence Mutualiste " Les Tilleuls "
  • Hôpital Broca
  • Résidence Mutualiste " La Cerisaie "
  • Résidence Mutualiste " Marie Lagrevol "

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Arm AB : Intervention under study x Control intervention

Arm BA: Control intervention x Intervention under study

Arm Description

Subjects receive intervention A during which they will benefit from a systemic pain assessment and from the PARO robot as a therapeutic mediator, followed by intervention B during which patients will benefit from a systemic pain assessment without the PARO robot.

Subjects receive intervention B during which they will benefit from a systemic pain assessment without the PARO robot, followed by intervention A during which patients will benefit from a systemic pain assessment and from the PARO robot as a therapeutic mediator.

Outcomes

Primary Outcome Measures

ALGOPLUS scale
A proximal measure of pain rating on a scale of 1) facial expressions, 2) look, 3) complaints, 4) body position and, 5) atypical behaviors. And a distal measures of pain

Secondary Outcome Measures

PACSLAC-F score
A distal measure of pain .
PACSLAC-F score
A distal measure of pain .
PACSLAC-F score
A distal measure of pain .
Simple verbal scale (SVS)
Measurement with a scale in 3 points
The appreciation of the Paro robot
Measurement with a visual scale in 5 points: from 1 (not at all) to 5 (considerably) on a visual scale.
Incidence of patient Medication
Medications (analgesic, neuroleptic, anxiolytic, antidepressant, sleeping pill) taken by the patient
EQ-5D score
A questionnaire (EQ-5D) of quality life which includes five single-item dimensions assessing: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression of participants.
EQ-5D score
A questionnaire (EQ-5D) of quality life which includes five single-item dimensions assessing: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression of participants.
EQ-5D score
A questionnaire (EQ-5D) of quality life which includes five single-item dimensions assessing: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression of participants.
Appreciation of care
Measurement with 2 visual scales in 4 and 5 points
Appreciation of PARO robot
Measurement with a visual scale in 5 points
Duration of the care
NASA-TLX score
The NASA-TLX is an instrument to assess overall subjective workload with 6 dimensions of "workload" experienced by the health-care team: Mental Demand, Physical Demand and Temporal Demand, Frustration, Effort, and Performance

Full Information

First Posted
July 9, 2018
Last Updated
November 19, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
The Paul Bennetot Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03591822
Brief Title
Pilot Study of a Robot-assisted Intervention for the Management of Care-induced Pain in Dementia
Acronym
PARODOL
Official Title
Prevention of Care-induced Pain in Elderly Persons With Cognitive Impairments and Living in EHPAD : Systematic Evaluation and Mediation With the PARO Robot.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
February 15, 2019 (Actual)
Primary Completion Date
April 12, 2019 (Actual)
Study Completion Date
April 12, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
The Paul Bennetot Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Health care professionals lack tools to deal with acute pain in patients with moderate to severe dementia during daily nursing situations. Care-induced pain in institutionalized persons with cognitive impairments can cause anxiety and behavioral problems.The aim of this study is to demonstrate that a systematic identification of pain associated with the use of social robots such as the PARO robot may contribute to a better anticipation and management of care-induced pain. The investigators hypothesize that an individual use of the PARO robot would bring relaxation to the patient, a distraction regarding the aversive situation of care and, thus, it would prevent manifestations of acute pain in patients with dementia. Secondary objectives of the study : determine the effect of the use of PARO during painful cares on quality of life, medication of patients, and perceived workload of the health-care team. examine socio-demographic and clinical responders' participants to the intervention, and, identify essential elements regarding cost-effectiveness of a systematic evaluation of pain and a mediation with the PARO robot in care-induced pain
Detailed Description
in is a frequent problem in persons with moderate to severe dementia and has been associated to different care situations. Daily observations in care homes show that pain frequently causes anxiety and behavioral symptoms, including agitation and opposition to nursing care. A key recommendation of the International Psychogeriatric Association (IPA) is the use of psychosocial approaches as first-line therapy for behavioral problems in persons with dementia. Indeed, a wide range of non-pharmacological interventions for persons with dementia exist, such as biofeedback, music therapy, therapeutic touch or relaxation. Most of these interventions have shown positive results on health status, quality of life, socialization, and functional capacity in dementia. However, to date, little is known on the effect of psychosocial interventions on care-induced pain in this population. In consequence, there is still a need for the development of innovative interventions. At a time when modern technologies are assuming a central role in our society, investigators are currently witnessing an important evolution of the use of social robots in healthcare interventions. In this research area, numerous studies have been conducted with social robots, such as PARO®, an animal-like robot modeled on a baby harp seal. Most of them have been successful in encouraging communication and/or social behaviors and also reducing Behavioral and Psychological Symptoms of Dementia (BPSD), loneliness, stress' levels, agitation and the use of pain medication. However, although these results indicate a potential application of robot-assisted therapies for pain management in persons with dementia, the use of PARO during painful care-situations is still to be investigated. The investigators propose a new combination of current health cares, namely to mediate care-induced pain with the PARO robot. Consequently, a randomized AB/BA crossover design will be employed. Patients will be assigned randomly to either phase A during which they will benefit from a systemic pain assessment and from the PARO robot as a therapeutic mediator, followed by phase B during which patients will benefit from a systemic pain assessment without the PARO robot, or phase B followed by phase A.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Moderate to Severe Dementia
Keywords
Dementia, Pain, Nursing care, Psychosocial intervention, Robot-assisted therapy, paro robot

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm AB : Intervention under study x Control intervention
Arm Type
Other
Arm Description
Subjects receive intervention A during which they will benefit from a systemic pain assessment and from the PARO robot as a therapeutic mediator, followed by intervention B during which patients will benefit from a systemic pain assessment without the PARO robot.
Arm Title
Arm BA: Control intervention x Intervention under study
Arm Type
Other
Arm Description
Subjects receive intervention B during which they will benefit from a systemic pain assessment without the PARO robot, followed by intervention A during which patients will benefit from a systemic pain assessment and from the PARO robot as a therapeutic mediator.
Intervention Type
Behavioral
Intervention Name(s)
A : Systemic evaluation of the pain and mediation with the PARO therapeutic robot
Intervention Description
Each session with the PARO robot will encompasses the same four following steps (a) Meeting Paro (b) Proposing contact (c) Individually using Paro during the care (d) End of the exposure.
Intervention Type
Behavioral
Intervention Name(s)
B : Systemic evaluation of the pain
Intervention Description
A systematic evaluation of the pain
Primary Outcome Measure Information:
Title
ALGOPLUS scale
Description
A proximal measure of pain rating on a scale of 1) facial expressions, 2) look, 3) complaints, 4) body position and, 5) atypical behaviors. And a distal measures of pain
Time Frame
2 months
Secondary Outcome Measure Information:
Title
PACSLAC-F score
Description
A distal measure of pain .
Time Frame
at inclusion
Title
PACSLAC-F score
Description
A distal measure of pain .
Time Frame
4 weeks
Title
PACSLAC-F score
Description
A distal measure of pain .
Time Frame
8 weeks
Title
Simple verbal scale (SVS)
Description
Measurement with a scale in 3 points
Time Frame
2 months
Title
The appreciation of the Paro robot
Description
Measurement with a visual scale in 5 points: from 1 (not at all) to 5 (considerably) on a visual scale.
Time Frame
2 months
Title
Incidence of patient Medication
Description
Medications (analgesic, neuroleptic, anxiolytic, antidepressant, sleeping pill) taken by the patient
Time Frame
2 months
Title
EQ-5D score
Description
A questionnaire (EQ-5D) of quality life which includes five single-item dimensions assessing: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression of participants.
Time Frame
at inclusion
Title
EQ-5D score
Description
A questionnaire (EQ-5D) of quality life which includes five single-item dimensions assessing: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression of participants.
Time Frame
4 weeks
Title
EQ-5D score
Description
A questionnaire (EQ-5D) of quality life which includes five single-item dimensions assessing: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression of participants.
Time Frame
8 weeks
Title
Appreciation of care
Description
Measurement with 2 visual scales in 4 and 5 points
Time Frame
2 months
Title
Appreciation of PARO robot
Description
Measurement with a visual scale in 5 points
Time Frame
2 months
Title
Duration of the care
Time Frame
2 months
Title
NASA-TLX score
Description
The NASA-TLX is an instrument to assess overall subjective workload with 6 dimensions of "workload" experienced by the health-care team: Mental Demand, Physical Demand and Temporal Demand, Frustration, Effort, and Performance
Time Frame
2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient over 60 years of age Consent to participate Patient diagnosed by a geriatrician or a neurologist with moderate to severe dementia (MMSE<24), according to the criteria of the Diagnostic and Statistical Manual DSM IV-TR (APA,2004) and NINCDS-ADRDA(McKhann et al.1984). Patient living in a nursing home or a long stay department Painful patient during nursing care (pain drugs prescription or direct observation) Exclusion Criteria: Patient (or patient's legal representative) does not provide consent The presence of acute organic disease or psychiatric decompensation and major neuropsychiatric symptoms incompatible with the intervention. Patient who cannot interact physically with Paro The presence of multidrug-resistant bacteria in patient to reduce the risk of contamination.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne-Sophie RIGAUD, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Résidence Mutualiste " L'adret "
City
Bellegarde En Forez
ZIP/Postal Code
42210
Country
France
Facility Name
Résidence Mutualiste " Les Tilleuls "
City
La Grand Croix
ZIP/Postal Code
43320
Country
France
Facility Name
Hôpital Broca
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Résidence Mutualiste " La Cerisaie "
City
Saint Etienne
ZIP/Postal Code
42000
Country
France
Facility Name
Résidence Mutualiste " Marie Lagrevol "
City
Saint-just-malmont
ZIP/Postal Code
43240
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Pilot Study of a Robot-assisted Intervention for the Management of Care-induced Pain in Dementia

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