№ lp_2_1_11933
File format: docx
Character count: 17726
File size: 137 KB
Year:
2025
Region / City:
Muncie, IN
Topic:
Education, Special Education, Teacher Training
Document Type:
Course Syllabus
Institution:
Ball State University
Instructor:
Dr. Brittany Bales
Target Audience:
Students in Teacher Education Program
Prerequisites:
SPCE 375 with a grade of C or better; overall GPA of 3.0 or better
Course Period:
Fall 2025
Approval Date:
Not specified
Changes Date:
Not specified
Description:
A course syllabus outlining a practicum for students pursuing teaching certification for students with mild disabilities, with field experience and related assessments.
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Note:
Instructor Information
Instructor:
Geetika Agarwal, Ph.D., BCBA-D, QBA, LBA (Washington)
Institution:
Ball State University, Department of Special Education, Applied Behavior Analysis & Autism Program
Location:
Muncie, IN
Contact:
[email protected]
Office Hours:
Saturday 1 pm EST
Course Modality:
Online
Prerequisites:
Admission to the program
Duration:
16 weeks
Course Structure:
Includes examinations, online group discussions, and written assignments
Course Goals:
Gain understanding of ABA principles, behavior analysis, and data interpretation
PL01:
Apply behavioral foundations of ABA
PL02:
Apply ABA concepts in real-world settings
PL03:
Understand measurement and data interpretation for interventions
CO1:
Compare ABA with other behavior explanations
CO3:
Develop objective operational definitions
CO4:
Explain functional relationships in behavior
CO5:
Explain arranging consequences to increase behavior
CO6:
Explain arranging consequences to decrease behavior
CO7:
Discuss ethical issues with punishment procedures
CO8:
Develop stimulus control examples
CO9:
Demonstrate understanding of the four-term-contingency
CO10:
Understand matching law and reinforcement schedules
Year:
2015
Region / City:
Washington, D.C.
Topic:
Unemployment Insurance, Data Validation
Document Type:
Advisory
Agency / Organization:
U.S. Department of Labor, Employment and Training Administration
Author:
Portia Wu
Target Audience:
State Workforce Agencies
Period of Validity:
Until May 31, 2016
Approval Date:
May 2013
Date of Last Modification:
March 2016
Year of metadata update:
2024-12-20
Goal:
Goal 3: Ensure healthy lives and promote well-being for all at all ages
Target:
Target 3.6: By 2020, halve the number of global deaths and injuries from road traffic accidents
Indicator:
Indicator 3.6.1: Death rate due to road traffic injuries
Related indicators:
3.5; 11.2
Custodian agency:
World Health Organization
Data reporter:
World Health Organization
Definition:
Number of road traffic fatal injury deaths per 100,000 population
Numerator:
Number of deaths due to road traffic crashes
Denominator:
Population (number of people by country)
Unit of measure:
Per 100,000 population
Classification system:
International Classification of Diseases, Tenth Revision (ICD-10), Chapter XX: External Causes of Morbidity and Mortality (V01–V99)
Data sources:
Global Status Report on Road Safety survey; vital registration or certificate deaths data from ministries of health; population data from United Nations Department of Economic and Social Affairs, Population Division
Data collection method:
National multi-sectoral consultation coordinated by WHO Regional Advisors, Regional Data Focal Points and National Data Focal Points with consensus validation
Data collection frequency:
Annual request for cause-of-death statistics
Data release frequency:
Every two or three years (Global Status Report on Road Safety; latest 2023)
Data providers:
Ministry of health; ministry of interior; ministry of transport
Data compiler:
World Health Organization
Institutional mandate:
Article 64 of the WHO Constitution and WHO Nomenclature Regulations (1967)
Thematic area:
Public health; road safety; mortality statistics
Geographical coverage:
Global; WHO Member States
Year:
2024
Region / City:
Europe / Strasbourg, France; Slovakia; Paris, France; Krakow, Poland; Groningen, Netherlands; Louvain-la-Neuve, Belgium
Topic:
Social Psychology; European Scientific Community; Research Funding
Document Type:
Newsletter / Bulletin
Organization:
European Association of Social Psychology (EASP)
Author:
EASP Executive Committee; Nurit Shnabel (President)
Target Audience:
EASP members, doctoral students, European social psychologists
Period Covered:
April 2024–July 2026
Key Events:
EASP Summer School 2024, General Meeting 2026, Small Group Meetings April 2024
Membership Updates:
25 new full members, 81 new postgraduate members
Funding and Grants:
Recent grant reports, new grants awarded, Social Psychology Ambassadors program
Editorial Changes:
New editors at EJSP, European Studies in Social Psychology monograph series
Administrative Notes:
Membership database updates, payment registration, online voting for Supervisory Board
Mild to Moderate Support Needs Teaching Performance Expectations Comparison Chart Updated April 2021
Year:
2021
Region / City:
California
Topic:
Education
Document Type:
Educational Guidelines
Author:
Unknown
Target Audience:
Teacher Candidates, Education Specialists
Period of Validity:
Ongoing
Approval Date:
April 2021
Date of Modifications:
N/A
Note:
Year
Subject:
Sports injuries, Concussions
Document Type:
Acknowledgement Form
Target Audience:
Athletes, parents, sports organizations
Year:
2026
Region / City:
London Borough of Merton
Subject:
Referral Form for Learning Disability Services
Document Type:
Referral Form
Organization / Institution:
Merton Integrated Learning Disability Team (MILD)
Author:
Not specified
Target Audience:
Professionals referring individuals for support
Period of Action:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2025
Region / City:
Muncie, IN
Topic:
Education, Special Education
Document Type:
Course Syllabus
Institution:
Ball State University
Instructor:
Maria B. Sciuchetti
Target Audience:
Students enrolled in SPCE 686.800
Period of Validity:
Fall 2025
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2021
Region / City:
Alwarkurichi, Tamil Nadu, India
Field:
Corrosion Science
Document Type:
Research Article
Institution:
Sri Paramakalyani College, Alwarkurichi, Tamil Nadu
Author(s):
I. Malar Vizhi, Dr. S. Selvaraj, Dr. K. Kalirajan
Target Audience:
Researchers in corrosion science and materials engineering
Effective Date:
2021
Modification Date:
None
Document Type:
Template letter
Purpose:
Appeal of prior authorization denial
Product Name:
OPZELURA (ruxolitinib) cream 1.5%
Indication:
Mild to Moderate Atopic Dermatitis
Intended Author:
Prescriber
Intended Recipient:
Health Plan or Payer
Target Population:
Non-immunocompromised adult and pediatric patients 12 years of age and older
Subject Matter:
Coverage appeal and prescribing information
Included Sections:
Sample appeal letter, Indication, Limitations of Use, Important Safety Information
Medical Context:
Prior authorization denial and coverage review process
Year:
2023-2024
Region / City:
USA
Subject:
Special Education
Document Type:
Report
Organization / Institution:
ETS
Author:
ETS
Target Audience:
Educators, Policy Makers, Educational Institutions
Effective Period:
2023-2024
Approval Date:
Not specified
Date of Changes:
August 1, 2023
Year:
2024
Region / City:
Australia
Topic:
Psoriasis Treatment
Document Type:
Patient Handout
Organization:
Victorian Government, Department of Health
Author:
Not specified
Target Audience:
Patients with mild plaque psoriasis
Period of validity:
Not specified
Approval Date:
March 2024
Amendment Date:
Not specified
Cost Information:
Free consultation; medicine costs vary based on Medicare and PBS status
Eligibility:
Adults aged 18 or older with mild plaque psoriasis
Additional Support:
Websites provided for more information
Complaint Process:
Information on complaints available at www.health.vic.gov.au/feedback-and-complaints
Safety Net Information:
Medications not included in PBS Safety Net
Consultation Details:
Private consultation with a pharmacist
Prescription Information:
Medicines under PBS or full price for non-listed items
International Students:
Eligible based on specific countries
Consent Process:
Provided during consultation
Health Advice:
Self-care and lifestyle tips included
Expected Outcome:
Symptoms should improve within 2-4 weeks
What to do if symptoms worsen:
Visit a doctor if no improvement or worsening of condition
Contact:
[email protected]
Note:
Year
Context:
A document used to assess the functional capacity of an individual with mild brain impairment for disability support pension purposes.
Year:
2003
Program:
Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Type of document:
Supplementary research material
Research field:
Alzheimer’s disease and neurodegenerative disorders
Study type:
Longitudinal neuroimaging and biomarker study
Principal Investigator:
Michael W. Weiner, MD
Participant groups:
Cognitively normal (CN) participants; Mild cognitive impairment (MCI) participants
Participant age range:
55–90 years
Assessment methods:
MRI, PET, biological markers, clinical assessment, neuropsychological testing
Cognitive assessment tools:
Mini-Mental State Exam; Clinical Dementia Rating; Logical Memory II subscale of the Wechsler Memory Scale-Revised
Diagnostic focus:
Mild cognitive impairment and early Alzheimer’s disease progression
Language requirements for participants:
Fluent English or Spanish
Biological sampling:
Blood for genomic analysis and biomarkers; cerebrospinal fluid collection via lumbar puncture
Genomic analysis:
GWAS sequencing and APOE testing
Medication requirements:
Stability of permitted medications and washout from certain psychoactive medications prior to screening
Study participation requirement:
Availability of a study partner with regular participant contact
Imaging requirements:
Repeated MRI (3T) and at least two PET scans
Education requirement:
Minimum six grades of education or adequate work history
Exclusion criteria scope:
Neurologic diseases, psychiatric disorders, substance abuse history, MRI contraindications, unstable medical conditions
Year:
2025
Region / City:
United Kingdom
Topic:
Alzheimer’s Disease, Mild Cognitive Impairment, Dementia Treatment
Document Type:
Appeal
Organization / Institution:
Eli Lilly & Company Ltd
Author:
Eli Lilly & Company Ltd
Target Audience:
Healthcare professionals, Policy makers, Medical researchers
Period of Effectiveness:
Not specified
Approval Date:
23 October 2024
Date of Amendments:
12 June 2025
Topic:
Functional exercise assessment and metabolic equivalent estimation in mild COVID-19
Document type:
Clinical calculation example and methodological note
Medical test:
6-Minute Walk Test
Medical condition:
Coronavirus Disease 2019 (COVID-19)
Clinical parameter:
Metabolic Equivalents (METs)
Measurement units:
feet, meters, meters per minute, miles per hour, ml/kg/min
Example walking distance:
1400 feet in 6 minutes
Converted distance:
427 meters
Calculated walking speed:
71 m/min (2.65 miles/hour)
Estimated oxygen consumption:
10.6 ml/kg/min
Estimated MET level:
approximately 3 METs
Comparative example:
1850 feet in 6 minutes corresponding to approximately 3.7 METs and 94 m/min walking speed
Methodological constants:
1 MET = 3.5 ml/kg/min; conversion constant 0.1 for m/min to ml/kg/min
Field:
Clinical assessment and triage methodology
Year:
2014
Region / City:
Hamilton, Ontario
Theme:
Occupational therapy, Cognitive impairment, Memory clinic
Document type:
Thesis
Organization / Institution:
McMaster University
Author:
Laura Turner
Target Audience:
Healthcare professionals, researchers in cognitive health
Period of validity:
2014 onwards
Approval Date:
May 2014
Date of Changes:
Not specified
Year:
2023
Region / City:
Bristol
Topic:
Mild Cognitive Impairment Research
Document Type:
Research Study
Institution:
University of Bristol
Author(s):
Dr Nick Turner, Professor Liz Coulthard
Target Audience:
Individuals diagnosed with mild cognitive impairment in the last 12 months
Study Period:
Ongoing
Approval Date:
Not specified
Amendment Date:
Not specified
Funding:
National Institute for Health Research
Note:
Issue date
Scope:
Children and adults presenting with distress due to pain
Red Flags:
Suspected infection, Recent significant trauma
Indications:
Mild to moderate pain relief, Anti-inflammatory pain relief, Moderate pain relief with codeine
Medicines:
Paracetamol, Ibuprofen, Codeine phosphate
Dosage instructions:
See standing order for age-specific dosing
Route of administration:
Oral
Quantity:
Paracetamol 60 x 500mg tablets or 200mLs suspension, Ibuprofen 40 x 200mg tablets or 200mLs suspension, Codeine 12 x 15mg tablets
Contraindications:
Liver failure, Renal failure, Hypersensitivity to NSAIDs, Severe heart failure, Gastro-intestinal ulceration or bleeding, Acute respiratory depression
Precautions:
Elderly, cardiac impairment, hypertension, risk of sedation, constipation, dependence, drug-seeking behavior
Follow-up:
Return if pain is uncontrolled, worsens, or symptoms change
Countersigning and auditing:
Countersigning required within 48 hours for orders including codeine
Competency/training requirements:
Nurses must be signed off as competent and trained for this standing order
Supporting documentation:
Healthpathways, Best Practice Journal, New Zealand Formulary, Medsafe data sheets, Standing Order Guidelines Ministry of Health 2012, Medicines (Standing Order) Regulations 2012
Signed by issuer:
Name, Title, Date