Meaningful Activity Intervention for Persons With Mild Cognitive Impairment

• ClinicalTrials.gov Identifier: NCT01843283
• Recruitment Status: Completed
• First Posted: April 30, 2013
• Last Update Posted: October 25, 2016
• Sponsor: Indiana University
• Information provided by (Responsible Party): Indiana University

Study Description

Brief 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.

Condition or disease	Intervention/treatment	Phase
Mild Cognitive Impairment	Behavioral: Daily Enhancement Meaningful Activity (DEMA); Behavioral: Information Support (IS)	Phase 1

Detailed 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.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 80 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Outcomes Assessor)
• Primary Purpose: Supportive Care
• Official Title: Meaningful Activity Intervention for Persons With Mild Cognitive Impairment
• Study Start Date: July 2012
• Actual Primary Completion Date: March 2015
• Actual Study Completion Date: May 2016

Arms and Interventions

Arm	Intervention/treatment
Experimental: Daily Enhancement Meaningful Activity (DEMA); The group member will receive Self-management Toolkit and 6 bi-weekly individualized sessions, 2 face-to-face and 4 via telephone delivered by a trained intervener. DEMA will provide autonomy support by helping patients to identify and prioritize activities, classify needs and goals, generalize manageable solutions, engage in self-selected activities under family support, and self-evaluate failure and success or renew problem-solving as needed.	Behavioral: Daily Enhancement Meaningful Activity (DEMA)
Active Comparator: Information Support (IS); The IS group will receive 2 face-to-face meetings to receive an overview of what will happen in the study and an initial Alzheimer Association, educational brochure. Then they will receive 4 biweekly follow-up phone calls and have the opportunity to ask only questions related to the educational materials.	Behavioral: Information Support (IS)

Outcome Measures

Primary Outcome Measures :

1. Patient_Depression symptoms: Patient Health Questionnaire Depression Scale (PHQ-9) [ Time Frame: Change in depression from baseline to immediately (two-week)- and 3 months post-intervention ]

Secondary Outcome Measures :

1. Patient_satisfaction with communication: The subscale of Communication and Affective Responsiveness [ Time Frame: Change in satisfaction with communication from baseline to immediately (two-week)- and 3 months post-intervention ]
2. Patient_Physical Function: Alzheimer disease cooperative study activities of daily living inventory. [ Time Frame: Change in physical function from baseline to immediately (two-week)- and 3 months post-intervention ]
3. Patient_Life satisfaction : Life Satisfaction Index for the Third Age-Short Form [ Time Frame: Change in life satisfaction from baseline to immediately (two-week)- and 3 months post-intervention ]
4. Patient_Satisfaction with program: Satisfaction with Meaningful Activity Program Scale is adapted from the Caregiver Satisfaction Scale [ Time Frame: It will be collected at 3 months post-program evaluation ]
5. Patient_ Meaningful activities engagement performance and satisfaction: Canadian Occupational Performance Measure & weekly log [ Time Frame: Change in meaningful activities engagement performance and satisfactionfrom baseline to immediately (two-weeks)- and 3 months post-intervention ]
6. Patient_Sense of confidence: Confidence Scale [ Time Frame: Change in sense of confidence from baseline to immediately (two-week)- and 3 months- post program ]
7. Caregiver_Depressive Symptoms: PHQ-9 [ Time Frame: Change in depressive symptoms from baseline to immediately (two-week)- and 3 months post-program evaluation ]
8. Caregiver_ Caregiver life changes: Caregiving Outcomes Scale [ Time Frame: Change in caregivign outcomes from baseline to immediately (two-week)- and 3 months post-post program ]
9. Caregiver_- Satisfaction with program: Satisfaction with Meaningful Activity Program Scale is adapted from the Caregiver Satisfaction Scale [ Time Frame: It will be assessed at 3 months post-program evaluation ]

Eligibility Criteria

• Ages Eligible for Study: 21 Years to 95 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

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)

Contacts and Locations

Locations

United States, Indiana

Indiana University School of Nursing

Indianapolis, Indiana, United States, 46202

Sponsors and Collaborators

Indiana University

Investigators

• Principal Investigator: Yvonne Lu, PhD; IU School of Nursing

More Information

• Responsible Party: Indiana University
• ClinicalTrials.gov Identifier: NCT01843283
• Other Study ID Numbers: 1R21NR013755-01 ( U.S. NIH Grant/Contract )
• First Posted: April 30, 2013
• Last Update Posted: October 25, 2016
• Last Verified: October 2016

Keywords provided by Indiana University:

Mild Cognitive Impairment; Family Caregivers; Intervention studies

Additional relevant MeSH terms:

Cognitive Dysfunction; Cognition Disorders; Neurocognitive Disorders; Mental Disorders