Exercise and Activities for Independent Living With Mild Cognitive Impairment (MCI)

Dementia Clinical Trial

Official title:

Exercise & Health Promotion for MCI: A Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00446394
• Other study ID #: 30692-J
• Secondary ID: 2R01AG014777IA01
• Status: Completed
• Phase: N/A
• First received: March 8, 2007
• Last updated: October 18, 2012
• Start date: June 2007
• Est. completion date: October 2012

Study information

• Verified date: October 2012
• Source: University of Washington
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

The purpose of this project is to evaluate an exercise and health promotion program for older adults with mild memory loss. The study will investigate the efficacy of a memory-enhanced exercise and health promotion program to determine whether it is more effective than a social walking program in delaying further memory decline, improving mood and physical function, and enhancing quality of life.

Description:

This project is a randomized controlled trial to evaluate the efficacy of a group exercise and health promotion program designed specifically for older adults with Mild Cognitive Impairment (MCI). This study builds upon previous studies designed for cognitively intact older adults, with a supplemental study using a modified intervention for MCI participants, and for individuals with Alzheimer's disease.

Taken together, these prior investigations support the efficacy of behaviorally based exercise interventions in improving cognitive, physical, and affective status in cognitively intact and demented older adults. Results from a feasibility study suggest that these positive outcomes can also be obtained in older adults with MCI.

The current study will investigate the efficacy of the modified exercise program called RALLI (Resources and Activities for Life Long Independence) to determine whether it is more effective than the control condition, a social walking program (SW), in delaying cognitive decline, improving self-rated health and health behaviors, improving affect and physical function, and enhancing quality of life. The long-term efficacy of RALLI to delay conversion of MCI to dementia, reduce physical disability, maintain independent living, and improve physiological health indicators will also be investigated.

One hundred seventy participants over the age of 70 who meet American Academy of Neurology criteria for MCI will be recruited from independent living retirement residences. Participants will be randomly assigned to one of the two conditions (RALLI and SW) and assessed at baseline, post treatment (3 months), and follow up visits every 6 months for a total of 3 years (months 6, 12, 18, 24, 30, and 36). The hypothesis is that RALLI participants will experience better post-treatment outcomes than SW participants, and that gains will be maintained over 36 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 181
• Est. completion date: October 2012
• Est. primary completion date: October 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 70 Years and older

Eligibility

Inclusion Criteria:

• Mild Cognitive Impairment defined as

• - Memory complaint

• - Objective memory impairment for age and education

• - Largely intact general cognitive function

• - Essentially preserved activities of daily living

• - Not already diagnosed with dementia

• Insufficient physical activity defined as less than 150 minutes per week of moderate intensity physical activity

• Not currently in an exercise program similar to the study program

Exclusion Criteria:

• Not ambulatory

• Expected to move from the study geographic area during the study period

• Have a known terminal illness

• Actively suicidal, hallucinating, or delusional

• Hospitalized for a psychiatric disorder in the 12 months before baseline

• Uncontrolled chronic conditions, e.g. uncontrolled hypertension, unstable angina, uncontrolled blood glucose

• Blind or deaf

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cognition Disorders
• Dementia
• Mild Cognitive Impairment

Intervention

Behavioral:
• Resources and Activities for Life Long Independence (RALLI)
Strengthening exercises, encouragement to walk daily, pedometer reading, health promotion information for 1.5 hours weekly for 9 weeks
• Social Walking program (SW)
Group support for walking, pedometer reading, 1 hour weekly for 9 weeks

Locations

Country	Name	City	State
United States	Northwest Research Group on Aging, Department of Psychosocial and Community Health, University of Washington School of Nursing	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in cognitive status		baseline, 3, 6, 12, 18, 24, 30, and 36 months	No
Secondary	Changes in health, affective, and functional status		baseline, 3, 6, 12, 18, 24, 30, and 36 months	No