Meaningful Activity Intervention for Persons With Mild Cognitive Impairment

Mild Cognitive Impairment Clinical Trial

Official title:

Meaningful Activity Intervention for Persons With Mild Cognitive Impairment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01843283
• Other study ID #: 1R21NR013755-01
• Status: Completed
• Phase: Phase 1
• First received: April 26, 2013
• Last updated: October 24, 2016
• Start date: July 2012
• Est. completion date: May 2016

Study information

• Verified date: October 2016
• Source: Indiana University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this pilot study is to evaluate the feasibility of and satisfaction with the revised DEMA and to estimate effect sizes for DEMA through incorporation of a comparison group. Specific aims are as follows:

Aim 1: Evaluate feasibility of the study for MCI patient/caregivers. Aim 2: Estimate effect sizes for DEMA on MCI patient and caregiver outcomes. Aim 3: Evaluate MCI patients and family caregivers' satisfaction with and perceptions of DEMA or IS.

Description:

Mild cognitive impairment (MCI) affects as many as 20% of older adults who are at a greater risk of developing Alzheimer's disease (AD). MCI involves functional decline that may include decrements in engagement in meaningful activities and one's own sense of confidence/mastery, and it is associated with depressive symptoms, poor satisfaction with family communication, and declining physical function. Existing interventions for MCI patients and caregivers often focus on a single problem, such as memory or physical activity and there are no available multi-faceted supportive care interventions to meet the needs of the MCI patients and their caregivers in order to prevent premature disengagement and risk for depressive symptoms. The Daily Enhancement of Meaningful Activity (DEMA) intervention uses a family dyadic, strengths-based, and positive health approach that builds on existing dyadic skills and values to accomplish meaningful activity engagement to address the priority needs for efficacious interventions to prevent premature disengagement and depressive symptoms in MCI patients. The DEMA builds on the investigators' previous descriptive work and gerontology theory, the model human occupation, and components of the Problem-Solving Therapy. The investigators' preliminary findings showed that the intervention and measures were acceptable, and suggestions were solicited from the participants for improving delivery. The purpose of this pilot study is to 1) evaluate the feasibility and satisfaction of the revised DEMA intervention; and 2) estimate effect sizes for the intervention through the incorporation of a comparison group. The MCI-caregiver dyads (n = 36 dyads) will be randomized to the DEMA or informational support groups; each group will receive 6 bi-weekly sessions (2 face-to-face and 4-phone delivered) with a trained intervener. The data from MCI patients and caregivers outcomes will be collected at pre-intervention, immediately (two weeks) post-intervention, and 3 months post-program evaluation. Descriptive statistics analysis will be used for satisfaction with and perception of the DEMA or informational support groups and general linear mixed models will be used to estimate the effect sizes of the intervention on the proximal and distal outcomes. Findings will inform the design of a subsequent R01 to: 1) test the efficacy of DEMA for MCI patient-caregiver dyads in a longitudinal randomized clinical trial; and 2) explore the costs/benefits of implementation. If it is found to be efficacious, DEMA has the potential to slow the rate of disability progression from MCI to AD and improve quality of life outcomes for patients and caregivers.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: May 2016
• Est. primary completion date: March 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 21 Years to 95 Years

Eligibility

Inclusion Criteria:

MCI patients:

1. are aged 60 years or older,

2. speak English,

3. have both caregiver-reported, clinically significant decline in cognition and clinician-detected or research based cognitive impairment on the standardized health exam

4. have at least one cognitive assessment score below the 7th percentile

5. have a normal range in performance of daily living tasks based on informant interview information indicating that impairment does not rise to the level of dementia.

Family caregivers:

1. are adults = 21 years of age;

2. have primary responsibility for providing unpaid care to an MCI relative, along with monitoring safety and providing social support

3. are able to read and speak English

4. are oriented to persons, places, and time [having a 6-item Mini-Mental State Examination (MMSE) score of 4 or above]

Exclusion Criteria:

MCI patients and family caregivers will be excluded if:

1. the MCI patient or family caregiver has a diagnosed bipolar disorder or untreated schizophrenia;

2. the family caregiver has significant cognitive impairment that may hinder participation (6-item MMSE < 4)

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Cognition Disorders
• Mild Cognitive Impairment

Intervention

Behavioral:
• Daily Enhancement Meaningful Activity (DEMA)

• Information Support (IS)

Locations

Country	Name	City	State
United States	Indiana University School of Nursing	Indianapolis	Indiana

Sponsors (1)

Lead Sponsor	Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient_Depression symptoms: Patient Health Questionnaire Depression Scale (PHQ-9)		Change in depression from baseline to immediately (two-week)- and 3 months post-intervention	No
Secondary	Patient_satisfaction with communication: The subscale of Communication and Affective Responsiveness		Change in satisfaction with communication from baseline to immediately (two-week)- and 3 months post-intervention	No
Secondary	Patient_Physical Function: Alzheimer disease cooperative study activities of daily living inventory.		Change in physical function from baseline to immediately (two-week)- and 3 months post-intervention	No
Secondary	Patient_Life satisfaction : Life Satisfaction Index for the Third Age-Short Form		Change in life satisfaction from baseline to immediately (two-week)- and 3 months post-intervention	No
Secondary	Patient_Satisfaction with program: Satisfaction with Meaningful Activity Program Scale is adapted from the Caregiver Satisfaction Scale		It will be collected at 3 months post-program evaluation	No
Secondary	Patient_ Meaningful activities engagement performance and satisfaction: Canadian Occupational Performance Measure & weekly log		Change in meaningful activities engagement performance and satisfactionfrom baseline to immediately (two-weeks)- and 3 months post-intervention	No
Secondary	Patient_Sense of confidence: Confidence Scale		Change in sense of confidence from baseline to immediately (two-week)- and 3 months- post program	No
Secondary	Caregiver_Depressive Symptoms: PHQ-9		Change in depressive symptoms from baseline to immediately (two-week)- and 3 months post-program evaluation	No
Secondary	Caregiver_ Caregiver life changes: Caregiving Outcomes Scale		Change in caregivign outcomes from baseline to immediately (two-week)- and 3 months post-post program	No
Secondary	Caregiver_- Satisfaction with program: Satisfaction with Meaningful Activity Program Scale is adapted from the Caregiver Satisfaction Scale		It will be assessed at 3 months post-program evaluation	No