Therapeutic Effects of Animal-assisted Therapy for Patients in a Minimally Conscious State (MCS Therapy)
Primary Purpose
Minimally Conscious State
Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Animal-assisted therapy
Conventional therapy
Sponsored by
About this trial
This is an interventional treatment trial for Minimally Conscious State
Eligibility Criteria
Inclusion Criteria:
- Inpatients of REHAB Basel in a minimally conscious state
- Minimum age of 18 years
- Informed consent documented by signature by the patient's legal representative
Exclusion Criteria:
- Medical contraindications for contact with animals such as allergy, phobia etc.,
- Enrollment of the investigator, his/her family members, employees and other dependent persons.
Sites / Locations
- REHAB BaselRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Animal-assisted therapy
treatment as usual
Arm Description
Patients receive three weeks of two AAT sessions, each lasting ca 30 minutes.
Patients receive three weeks of two control sessions, each lasting ca 30 minutes.
Outcomes
Primary Outcome Measures
Amount of goal achievement l: CSR-R
The goal achievement will be assessed via the JFK Coma Remission Scale revised (CSR-R), with 6 subscales and a total score ranging from 0 to 23 with higher scores indicating better outcomes.
Amount of goal achievement II: BAVESTA
The goal achievement will be assessed via the Basler Vegetative State Assessment. The scale ranges from 0 to 5 with higher scores indicating better outcomes.
Amount of goal achievement III: VAS
The goal achievement will also be assessed via a Visual Analogue Scale where a cross can be made on a line (measured in millimeters, ranging from 0 to 25) with higher values indicating better outcome.
Secondary Outcome Measures
Behavioral reactions
Behaviour of the patients will be coded in Noldus Observer according to a strict ethogram. State behaviours will be reported in % (relative to the duration of a session) and count behaviours as total number of shown behaviours during a session.
Heart rate
Heart rate will be measured in peats per minute using a Polar belt. HR is reported in beat per minutes (bpm).
Heart rate variability
Heart rate variability will be measured using a Polar belt. HRV is reported as mean RR intervals. The following HRV parameters will be calculated: time domain: the standard deviation of all normal-to-normal RR intervals (SDNN, ms) and root-mean square differences of successive RR intervals (RMSSD, ms); and frequency domain: relative power of the low frequency (LF) and high frequency (HF) band in normal units
Electrodermal activity (Galvanic Skin Response)
Electrodermal activity will be measured using the EMBRACE wristband. The outcome is reported in Microsiemens (sampling rate of 4Hz).
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03910959
Brief Title
Therapeutic Effects of Animal-assisted Therapy for Patients in a Minimally Conscious State
Acronym
MCS Therapy
Official Title
Therapeutic Effects of Animal-assisted Therapy for Patients in a Minimally Conscious State: a Randomized, Controlled Cross-over Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 10, 2019 (Actual)
Primary Completion Date
April 30, 2023 (Anticipated)
Study Completion Date
April 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Basel
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of this study is to investigate the effects of animal-assisted occupational therapy on patient's consciousness, measured via the achievement of predefined, patient-specific goals.
30 patients in a minimally conscious state will be included in this trial with randomized, controlled cross-over design. Patients will be randomized and allocated to either study arm 1 or 2 with an allocation ratio 1/1. In study arm 1, patients (N=15) receive three weeks of two AAT sessions per week followed by three weeks of two control sessions (TAU) per week. In study arm 2, patients (N=15) receive three weeks of two control sessions (TAU) per week followed by three weeks of two AAT sessions per week. Each session lasts 30 minutes. Goal attainment and secondary outcomes will be measured before the study start (pre-measurement, t0), at the end of the first 3 weeks therapy (post-measurement I, t1), at the start of the second 3 weeks (pre-measurement II, t2) as well as at the study end (post-measurement II, t3).
Detailed Description
Early rehabilitation is crucial for patients in a minimally conscious state (MCS). The reorganization of neuronal structures and the recovery of cognitive processes as well as emotional and physical functions are most important. To reach these goals, animal-assisted therapy (AAT) is part of the therapeutic concept at REHAB Basel. Regarding the results of our previous studies at REHAB Basel, patients with brain-injuries can profit from animal-assisted therapy in terms of socioemotional skills and therapy motivation. Furthermore, patients with severe disorder of consciousness showed more behavioural reactions and arousal during AAT compared to standard therapy sessions. However, there is no research investigating if AAT can help to facilitate reaching rehabilitation goals in patients in a MCS and therefore advance neurorehabilitation. Hence, this study investigates if animal-assisted occupational therapy can facilitate attainment of therapeutic goals.
The main outcome is the amount of achievement of predefined, patient-specific therapeutic goals. This will be measured via the JFK Coma Remission Scale revised (CSR-R), the Basler Vegetative State Assessment (BAVESTA) and on a goal attainment scale in %, filled out by the therapist.
Secondary outcomes are:
Behavioural reactions via behavioral video coding
Heart rate, Heart rate variability (HR/HRV)
Electrodermal activity (EDA) / Galvanic skin response (GSR)
The investigators will include 30 patients fulfilling the following inclusion criteria: Inpatients of REHAB Basel in a minimally conscious state (defined via the CRS-R according to the Aspen criteria); Minimum age of 18 years; Informed consent documented by signature by the patient's legal representative. The presence of any one of the following exclusion criteria will lead to exclusion of the participant: Medical contraindications for contact with animals such as allergy, phobia etc.); Enrollment of the investigator, his/her family members, employees and other dependent persons.
The study has a randomized, controlled cross-over design including 30 patients in a minimally conscious state. Patients will be randomized and allocated to either study arm 1 or 2 with an allocation ratio 1/1. In study arm 1, patients (N=15) receive three weeks of two AAT sessions per week followed by three weeks of two control sessions (TAU) per week. In study arm 2, patients (N=15) receive three weeks of two control sessions (TAU) per week followed by three weeks of two AAT sessions per week. Each session lasts 30 minutes. Before starting the study arm 1 or 2 therapists will define individual therapy goals for each patient.
Measurements will be taken before the study start (pre-measurement, t0), at the end of the first 3 weeks therapy (post-measurement I, t1), at the start of the second 3 weeks (pre-measurement II, t2) as well as at the study end (post-measurement II, t3).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Minimally Conscious State
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
The study has a randomized, controlled cross-over design.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Animal-assisted therapy
Arm Type
Experimental
Arm Description
Patients receive three weeks of two AAT sessions, each lasting ca 30 minutes.
Arm Title
treatment as usual
Arm Type
Active Comparator
Arm Description
Patients receive three weeks of two control sessions, each lasting ca 30 minutes.
Intervention Type
Other
Intervention Name(s)
Animal-assisted therapy
Intervention Description
Therapy in the presence and with interaction with an animal. Involved animals can be all species that live at REHAB Basel and are part of the AAT program. All animals are trained for the specific service with vulnerable patients.
Intervention Type
Other
Intervention Name(s)
Conventional therapy
Intervention Description
Parallelled conventional therapy sessions (treatment as usual)
Primary Outcome Measure Information:
Title
Amount of goal achievement l: CSR-R
Description
The goal achievement will be assessed via the JFK Coma Remission Scale revised (CSR-R), with 6 subscales and a total score ranging from 0 to 23 with higher scores indicating better outcomes.
Time Frame
3 weeks
Title
Amount of goal achievement II: BAVESTA
Description
The goal achievement will be assessed via the Basler Vegetative State Assessment. The scale ranges from 0 to 5 with higher scores indicating better outcomes.
Time Frame
3 weeks
Title
Amount of goal achievement III: VAS
Description
The goal achievement will also be assessed via a Visual Analogue Scale where a cross can be made on a line (measured in millimeters, ranging from 0 to 25) with higher values indicating better outcome.
Time Frame
3 weeks
Secondary Outcome Measure Information:
Title
Behavioral reactions
Description
Behaviour of the patients will be coded in Noldus Observer according to a strict ethogram. State behaviours will be reported in % (relative to the duration of a session) and count behaviours as total number of shown behaviours during a session.
Time Frame
3 weeks
Title
Heart rate
Description
Heart rate will be measured in peats per minute using a Polar belt. HR is reported in beat per minutes (bpm).
Time Frame
3 weeks
Title
Heart rate variability
Description
Heart rate variability will be measured using a Polar belt. HRV is reported as mean RR intervals. The following HRV parameters will be calculated: time domain: the standard deviation of all normal-to-normal RR intervals (SDNN, ms) and root-mean square differences of successive RR intervals (RMSSD, ms); and frequency domain: relative power of the low frequency (LF) and high frequency (HF) band in normal units
Time Frame
3 weeks
Title
Electrodermal activity (Galvanic Skin Response)
Description
Electrodermal activity will be measured using the EMBRACE wristband. The outcome is reported in Microsiemens (sampling rate of 4Hz).
Time Frame
3 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Inpatients of REHAB Basel in a minimally conscious state
Minimum age of 18 years
Informed consent documented by signature by the patient's legal representative
Exclusion Criteria:
Medical contraindications for contact with animals such as allergy, phobia etc.,
Enrollment of the investigator, his/her family members, employees and other dependent persons.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Karin Hediger, PhD
Phone
0041 79 519 78 85
Email
karin.hediger@unibas.ch
Facility Information:
Facility Name
REHAB Basel
City
Basel
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karin Hediger, Dr.
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Therapeutic Effects of Animal-assisted Therapy for Patients in a Minimally Conscious State
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