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Healthy Lifestyles for People With Intellectual Disabilities (HLID)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Willi Horner-Johnson, Oregon Health and Science University
ClinicalTrials.gov Identifier:
NCT00597948
First received: January 9, 2008
Last updated: February 23, 2012
Last verified: February 2012
  Purpose

Relatively few health promotion and disease prevention programs have included or targeted people with disabilities, and even fewer have focused on individuals with intellectual disabilities.

The long-term objectives of the Healthy Lifestyles for People with Intellectual Disabilities Study (HLID) are to increase the health of persons with intellectual disabilities by establishing the efficacy of a health promotion program and promoting its adoption. The HLID Study is based in the Center on Community Accessibility (CCA) at Oregon Health & Science University. The mission of CCA is to increase the health and health-related quality of life of persons with disabilities.

A pilot study conducted by CCA has established the effectiveness of the Healthy Lifestyles (HL) intervention among a cross-disability population in increasing health behavior adoption. The specific aim of the HLID Study is to test the efficacy of the HL program specifically with adults with intellectual disabilities.

The HLID Study uses a randomized control study design. The HL intervention will be administered to 75 adults and will compare results to those of an additional 75 adults who receive no intervention. Measurement will include anthropometric assessments to measure impacts on overweight and obesity, as well as self-report measures of healthy behaviors, health status, health care utilization, and secondary conditions. Results will be shared with research participants, presented through professional conferences and newsletters, and published in peer-reviewed journals with the assistance of community partners.


Condition Intervention
Mental Retardation
Developmental Disabilities
Intellectual Disabilities
Behavioral: Healthy Lifestyles Curriculum

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: Efficacy of a Health Intervention for People With Intellectual Disabilities

Resource links provided by NLM:


Further study details as provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):

Primary Outcome Measures:
  • Health Promoting Lifestyles Profile II [ Time Frame: Pre, post, and follow-up ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Body Mass Index (BMI) [ Time Frame: Pre, post, and follow-up ] [ Designated as safety issue: No ]
  • waist circumference [ Time Frame: pre, post, and follow-up ] [ Designated as safety issue: No ]
  • Community Integration Questionnaire [ Time Frame: pre, post, and follow-up ] [ Designated as safety issue: No ]
  • Healthy Lifestyles Knowledge Test [ Time Frame: pre, post, and follow-up ] [ Designated as safety issue: No ]
  • Starting and Continuing Healthy Behaviors [ Time Frame: pre, post, and follow-up ] [ Designated as safety issue: No ]
  • Self-Efficacy and Social Support for Activity for Persons with Intellectual Disabilities [ Time Frame: pre, post, follow-up ] [ Designated as safety issue: No ]
  • Living Well with a Disability Evaluation [ Time Frame: pre, post, follow-up ] [ Designated as safety issue: No ]
  • General Health Survey [ Time Frame: pre, post, follow-up ] [ Designated as safety issue: No ]
  • Healthy Lifestyles Goal Tracking Form [ Time Frame: post and follow-up ] [ Designated as safety issue: No ]

Enrollment: 131
Study Start Date: April 2007
Study Completion Date: March 2010
Primary Completion Date: January 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
Workshop Group: Receives Healthy Lifestyles curriculum and subsequent support.
Behavioral: Healthy Lifestyles Curriculum
Three consecutive days of six hours of training comprised of instruction and participant interaction.
No Intervention: 2
Comparison Group: Does not receive Healthy Lifestyles curriculum and subsequent support.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Living in Oregon or Southwest Washington
  • Ages 18-65 years
  • Have mild or moderate mental retardation/developmental disability/intellectual disability as defined by Oregon or Washington state (depending on place of residence) developmental disability service delivery system
  • Eligible in Oregon or Washington (depending on place of residence) to receive services for people with mental retardation/developmental/intellectual disability
  • Living in the community (i.e., group home, with family/friends, on own with or without support)
  • Participant defined health status of excellent, good, or fair
  • Participant expressed interest in participation in study
  • Participant expressed willingness to be assigned to either Workshop or Control study group
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00597948

Locations
United States, Oregon
Oregon Health & Science University
Portland, Oregon, United States, 97239
Sponsors and Collaborators
Investigators
Principal Investigator: Willi Horner-Johnson, Ph.D. Oregon Health and Science University/Center on Community Accessibility
  More Information

No publications provided

Responsible Party: Willi Horner-Johnson, Research Assistant Professor, Oregon Health and Science University
ClinicalTrials.gov Identifier: NCT00597948     History of Changes
Other Study ID Numbers: 1 R21 HD055189-01, 1 R21 HD055189-01
Study First Received: January 9, 2008
Last Updated: February 23, 2012
Health Authority: United States: Federal Government

Keywords provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):
developmental disability
developmental disabilities
intellectual disability
intellectual disabilities
mental retardation
downs syndrome
autism
autism spectrum disorder
cerebral palsy
health promotion
disease prevention
physical health
emotional health
behavioral health
mental health
spiritual health
prevention

Additional relevant MeSH terms:
Developmental Disabilities
Intellectual Disability
Mental Disorders Diagnosed in Childhood
Mental Disorders
Neurobehavioral Manifestations
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms

ClinicalTrials.gov processed this record on August 28, 2014