MOVE Curriculum: targetting kids, infant development programs, adults and students with orthopedic handicaps.
MOVE International
Linda Bidabe, MOVE administrator and creator, has
conducted training workshops in the United States, Europe,
Australia, New Zealand, Japan and South America. With new
hope, personal and professional caregivers flooded these
sessions. But the burdens and joys of liberating individuals
with severe disabilities are only now becoming understood.
Both learners and caregivers require further education,
guidance, reinforcement, new supportive equipment, proper
research, new techniques and new knowledge if exciting
progress is to continue to unfold.
MOVE International seeks to improve the overall quality of
life for people with severe disabilities and for the people
who care for them, regardless of age or cause of disability.
It also seeks to promote fuller participation in home, school,
work and community life and to encourage the dignity and hope
such participation brings to each individual.
Program Overview
MOVE is a top-down, activity-based curriculum designed to
teach students basic, functional motor skills needed for adult
life within the home and community environments. It combines
natural body mechanics with an instructional process designed
to help the students acquire increasing amounts of motoric
independence necessary for sitting, standing and walking. The MOVE curriculum provides a foundation for parental
leadership in the selection of student activities. The format
helps coordinate services provided by therapists, educators and
non-professionals.
Target Population
The program was originally designed to meet the needs of
children over age 7 who had not developed the physical skills
necessary to sit independently, bear weight on their feet, or
take reciprocal steps. Because of the worldwide success of the
program, the targeted population has been expanded to include
infant development programs, adults and students with orthopedic
handicaps only.
Early Beginnings
The need for this program became apparent when non-ambulatory
students began graduating from the public education system at
age 22 with fewer skills than when they entered at age 3. The
program was conceived after several surveys were conducted
concerning the needs of 100 students with the most severe physical
and cognitive delays. These students were between the ages of 3 and
22, but the majority were functioning below the six-month level of
development both physically and cognitively, according to the
Brigance Diagnostic Inventory of Early Development and the
developmental assessment according to Gessell. The results of
these surveys showed:
Communication Skills
Other than smiling or crying, the majority of the students had no
expressive language. Speech therapy which included augmentative and
alternative language training produced little or no change in
communication skills. The majority of the students appeared to have far
better receptive language than expressive language, i.e., many responded
by looking at the speaker to their names and words like Mama, bus, eat
and drink. A physical assessment was made of the students to determine
the most logical form of alternative communication. The students were then
introduced to a program developed at the Blair Learning Center to teach
students symbolic representation.
As an example of the program, the students were taught to
touch or look at a paper cup filled with their favorite liquid
to indicate the desire for a drink. When the student reached a
proficiency level, an empty paper cup was cut down until only the
circular bottom remained. It contained a picture of a cup, and the
student therefore was using symbolism to indicated the desire for a
drink. The same method was used for the category of food which began
with a real spoon with a favorite food and ended with a small picture
of a spoon. Using the same technique, varieties of food and drink were
offered. The shocking result of the program was that the students
who had any sort of mobility skills (crawling, rolling, squirming) were
able to succeed in the program and make meaningful choices. Those
students who lacked any sort of mobility were unable to make meaningful
choices. At that time, we did not know whether they were cognitively
unable to differentiate or whether they did not understand that they
had options.
Eating Skills
The majority of students with motor delays required
one-on-one assistance at meal time. Most of the students
had severe feeding problems complicated by chronic upper
respiratory distress. At minimum, a class of 10 students with
motor delays required five hours of adult assistance to
consume lunch (30 minutes per student). The most obvious
problems were lack of head control, tongue thrusting and an
uncoordinated swallow pattern.
Toileting Skills
Students under the age of 7 were routinely placed on
toilets. Toilet training efforts were reduced or completely
dismissed as students grew older, became heavier, or developed
deformities which made sitting difficult. When possible,
students had diapers changed on changing tables. As they
grew too large to be lifted safely, they were changed on
mats on the floor or in bean bags.
Large students with skeletal deformities took an average
of 20 minutes of adult assistance for a single diaper change
(2 adults X 10 minutes). A class of 10 large students with
motor delays required three hours and 20 minutes of adult
attendance for custodial care a minimum of twice a day.
Motor Skills
Therapy services were provided by the Kern County
California Children's Services (KCCCS) for those students who
had medically eligible diagnoses and were deemed capable of
making measurable progress in developmental activities. The
vast majority of the therapy services were delivered in the
"consultant" mode. That is, the therapist would discuss
the child's needs with the classroom teacher and instruct the
teacher in positioning and activities that would benefit
the person. The classroom teacher would then try to fit those
activities into the child's classroom day.
A number of articles published by E.E. Bleck, R.K. Beals
and others reported that children over the age of 7 who had
not gained independent motor skills by 7 were unlikely to ever
do so using traditional developmental programs based on the
sequential skill acquisition of infants. The students at the
Blair Learning Center supported these findings.
Home Life
Students who could be lifted and carried easily were taken
out into the community with the rest of the family. As the
students grew larger and more difficult to lift and transport,
they stayed at home more often. The majority of non-ambulatory
teenage students went into the community only to attend school
(via wheelchair bus) and for medical appointments. When the family
went out, one family member would stay at home with the
non-ambulatory person or occasionally a sitter was hired.
Sometimes, the non-ambulatory person was left unattended for
short periods of time.
Bathing was considered the most difficult task to be performed in
the home. Many students were bathed once a week in a bathtub or
shower and had sponge baths in bed the rest of the time. Usually the
student ate at different times than the rest of the family and often
ate in a reclining or semi-reclining position either in the living room
or bedroom. Diapers were often changed in the same environments because
moving the student was so difficult. The mother often slept with the
non-ambulatory student because of the periodic need for repositioning
or other attention during the night. Home environments as well
as community environments decreased in direct proportion to the
severity of physical handicaps and the size of the students.
School Life
The classes for students with severe handicaps averaged 10 students
per classroom with a teacher and an instructional aide. Between the
teacher and aide, 10 hours of instruction were available, which
if divided equally, gave each student 60 minutes. Students who were non
ambulatory and functioning below one year on the developmental scale
required one-on-one assistance for participation in any activity.
Lunch required a minimum of 30 minutes per student, and changing
diapers or toileting required an average of 10 minutes per change.
Custodial care (two diaper changes and lunch) required 50 of the 60
minutes available per day. Students who were too large to be
lifted by one person required even more of the available
instructional time. Additionally, many of the students with
severe physical disabilities required specialized procedures such
as putting on and removing braces, postural drainage, periodic
suctioning, etc. Instructional time decreased in direct
proportion to the severity of physical handicaps and the size
of the students.
Purposes Of The Program
MOVE is designed to:
-
Use education as a means of systematically
acquiring motor skills.
-
Use therapy services for cyclic corroboration,
i.e., therapists help establish an individual's
functional program, help train staff to use
the program, and periodically (on a cycle) work with
the individual and staff to update the program.
-
Provide a program whereby participants naturally
practice their motor skills while engaged in other educational
or leisure activities.
-
Reduce the time and energy requirements for custodial care.
-
Provide a way to measure small increments of functional
motor skills and therefore provide a way to show improvement.
-
Provide a sequence of motor skills which:
-
are age appropriate and based on a top-down model
of needs rather than the traditional developmental
programs based on sequential skills acquisition
of infants.
-
are valuable and usable to the participant right
now as well as in adulthood.
-
increase the availability of environments in the
community and in the home.
-
range from the level of zero self-management to
the level of independent self-management.
-
Provide the individual with the basic motor
skills needed for development of other skills such
as expressive language, self care and work opportunities.
MOVE is based on teaming the expertise of therapy and
education to address the functional needs of students when
they become adults. This teaming has resulted in the
development of equipment being manufactured by the Rifton
Manufacturing Company of Rifton, New York, which has been
designed specifically to meet the following needs:
The equipment places students in positions for performing
functional activities such as moving from one place
to another, self-feeding, self-controlled toileting,
table work and leisure activities
- The equipment allows the staff to physically manage
the student while teaching appropriate movement patterns
- The equipment allows the students to practice motor
skills independently
- The equipment is designed to help improve the bone
and joint health of the students and to increase the
muscle strength of the extensor musculature of the body
Eligibility For The Program
Exclusion from the program is limited to those individuals
whose medical needs contraindicate the need to sit, stand and
walk. Access to medical consultation and/or physical therapy
is needed for students who have the following conditions:
- Head too large to be supported by the neck
- Circulatory disease which prevents the participant
from being placed in a vertical position
- Respiratory distress
- Brittle bones
- Muscle contractures
- Curvature or rotation of the spine
- Hip dislocation
- Foot or ankle abnormalities
- Pain or discomfort in any part of the body
People with paralysis or degenerative neuromuscular
diseases can continue to participate to improve bone and
joint health for as long as it is medically feasible.
The Top-Down Model
The foundation for MOVE was laid by interviewing
parents about their children's needs and analyzing the
basic minimal activities necessary to adult functioning in
the home and community. Some of these activities
included:
IN THE HOME
- eating with family or peers
- bathing or showering
- getting in and out of bed
- dressing and grooming
- toileting
- communicating
- participating in leisure activities
IN THE COMMUNITY
- shopping
- going to appointments (medical, dental, hair dresser
or barber, etc.)
- eating in restaurants
- attending social activities indoors and out-of-doors
(church, picnics, movies, etc.)
- using public restrooms
- riding on public transportation or in regular cars
Task Analysis
Each of these activities was then task-analyzed
to determine the physical skills required in order to
accomplish these skills. The skills fell into 16 categories:
- Maintaining a sitting position
- Movement while sitting
- Standing
- Transition from sitting to standing
- Transition from standing to sitting
- Pivoting while standing
- Walking forward
- Transition from standing to walking
- Transition from walking to standing
- Walking backward
- Turning while walking
- Walking up steps
- Walking down steps
- Walking on even ground
- Walking up slopes
- Walking down slopes
Varying Levels of Success
Each of these 16 skills was then divided into four levels
of success. Each level has an immediate functional use and
will serve the needs of students in adulthood. When students
enter the program, they are given a top-down test developed
to serve their functional needs. The test begins with the
highest level of difficulty (GRAD LEVEL) and moves down a
continuum of skills until the student can demonstrate
proficiency. This is considered a student's entry level.
The student then addresses the next highest skill on the
continuum and disregards the skills below the entry level.
This system guarantees that students who learn slowly are
not wasting valuable time perfecting infant skills. The
four levels of success are:
- GRAD LEVEL - Acquisition of skills at this
level assures independent mobility in the home and minimal
assistance in the community. Participants who complete this
level graduate from the program and can expand their motor
skills through traditional programs. A wheelchair is never
needed.
- LEVEL I - Acquisition of skills at this level
assures that no lifting of the participant by the caretaker
will be required. The participant can walk with both hands
held or with a walkerette for a minimum of 300 feet.
A wheelchair is needed only for long distances.
- LEVEL II - Acquisition of skills at this level
assures that the participant will be able to walk at least
10 feet with help from another person in maintaining balance
and shifting weight. Lifting is minimal due to help from the
participant. A wheelchair is required for distances over
10 feet.
- LEVEL III - Acquisition of skills at this level
will improve bone health and functioning of internal organs
as well as decrease the likelihood of joint deformities and
pain. Three basic pieces of equipment were designed at the
Blair Learning Center to be used as prompts for skill
acquisition at this level. These include a front-leaning
chair which allows a student to assume a forward-leaning
position for table work, a mobile stander which is similar to
a wheelchair but places the student in a standing rather than
a sitting position, and a front-leaning walker which allows
an instructor to teach reciprocal leg movements without having
to support the student. These pieces of equipment are now
being manufactured by the Rifton Manufacturing Company and
are available worldwide.
Prompt Reduction System
The existing skills of the students are improved by selecting
the next higher skill from the top-down test and determining
exactly how much prompting the student needs to accomplish that
skill. Two categories of prompts are described in detail in the
MOVE Curriculum. One category is for learning to maintain sitting
balance and the other is for learning to stand and walk. These
prompts are given numerical values ranging from independent
functioning (0) to the greatest degree of assistance (5).
By using a simple chart, the instructor can see which areas
require the greatest degree of assistance and then systematically
reduce that assistance.