Cognitive Strategies for Improving Health Outcomes And Managing Risk Post-Stroke (CHAMPS)

September 12, 2024 updated by: Timothy P Dionne, University of New Mexico
The proposed research will further develop the CHAMPS intervention which is self-management intervention to learn new skills, despite current health status of experience a stroke. The study seeks to determine feasibility and compare pre- to post-intervention change including cardiovascular risk, quality of life, self-efficacy, recurrent stroke, hospital readmission, and perceived decline in health and function.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

People living with the effects of stroke frequently require assistance with everyday tasks (e.g., dressing, managing medications, driving) well-beyond 90-days post stroke. Executive function (EF) deficits are a major contributor to disability and as many as 75% of stroke survivors present with EF deficits. EF is a collection of cognitive processes that include orienting towards the future (i.e. planning), demonstrating self-control (i.e. behavioral inhibition), problem-solving, adapting to environmental changes, and facilitating goal-directed behaviors, all of which are essential skills for managing health. EF deficits are frequently undetected during hospitalization and result in discharge to the community with as many as 71% of survivors receiving inadequate services for long-term needs. Furthermore, scales of neurological impairment for classifying stroke severity like the NIH Stroke Scale (NIHSS) are frequently used as a standard of care and also sometimes support identification of impairments. However, research previously conducted by the research team indicates that this goes beyond the intended scope of the tools and scales like the NIHSS do not relate to EF deficits thus resulting in inadequate rehabilitation referrals if another EF screening or assessment is not used. Persons with post-stroke EF deficits have a multitude of modifiable risk factors that require intervention beyond regular health advice only. Consequently, the demand for specialized interventions to prevent and mitigate negative health outcomes (e.g., recurrent stroke, cardiovascular disease risk, cognitive decline risk, hospital readmission) in this population is quickly expanding and offers a significant opportunity for supporting recovery and improving quality of life for people with stroke. Although lifestyle-based vascular risk factor reduction interventions are numerous, there is a lack of consideration for targeting cognitive factors that can influence real-world application.

Study Type

Interventional

Enrollment (Actual)

8

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New Mexico
      • Albuquerque, New Mexico, United States, 87131
        • UNM Health Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. primary diagnosis of acute ischemic stroke within 90 days
  2. impairment of executive function (score >11 on Executive Interview)
  3. absence of severe aphasia (score of 0 or 1 on NIHSS will be included)
  4. absence of pre-stroke dementia (per client report)
  5. absence of major depressive disorder (PHQ-9 <14, Generalized Anxiety Disorder-7)
  6. absence of drug and alcohol misuse within 3 months of study admission (AUDIT)
  7. access to video-conference software on computer or device like computer tablet or smart phone
  8. >18 years of age

Exclusion Criteria:

  • Not fluent in English

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Feasibility Arm
A 10 sessions over 5 week virtual interaction between an occupational therapist and a person who is post-stroke, engage in meta-cognitive coaching to develop strategies to overcome barriers to daily living experienced in early stages of stroke. Outcomes anticipated are related to the American Heart Association's Healthy 8.
Cognitive Orientation to daily Occupational Performance is a performance-based treatment approach for children and adults who experience difficulties performing the skills they want to, need to or are expected to perform. Cognitive Orientation to daily Occupational Performance is a specifically tailored, active client-centered approach that engages the individual at the meta-cognitive level to solve performance problems. Focused on enabling success, the Cognitive Orientation to daily Occupational Performance Approach employs collaborative goal setting, dynamic performance analysis, cognitive strategy use, guided discovery, and enabling principles. These elements, all considered essential to the Cognitive Orientation to daily Occupational Performance Approach, are situated within a structured intervention format, and with parent/significant other involvement as appropriate.
Other Names:
  • Cognitive Orientation to daily Occupational Performance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Suitability and Feasibility Survey
Time Frame: 6 months
This survey will be conducted at the conclusion of study, to be completed by participants, examining whether this intervention is suitable and that the research protocols are feasible to be administered.
6 months
Battery of American Heart Association Life's Essential 8
Time Frame: 6 months

A battery of measures asking about the following:

  • Blood pressure
  • Weight and Height (BMI)
  • Blood sugar questions: Recently, has your doctor talked to you about managing your A1C?
  • Cholesterol, Cholesterol is a fatty substance found in the blood. About how long has it been since you last had your cholesterol checked? Have you ever been told by a doctor, nurse or other health professional that your cholesterol is high? Are you currently taking medicine prescribed by your doctor or other health professional for your cholesterol?
  • Smoking, recently, have you smoked or been around anyone who has smoked tobacco products?
  • Physical Activity, How active do you consider yourself? At least 150 minutes a week to be considered active
  • Sleep, How would you describe your sleep?
  • Diet, How would describe your diet?
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
NIH Stroke Scale
Time Frame: 6 months

National Health Stroke Scale:

15 items assessing severity of impairment in LOC, ability to respond to questions and obey simple commands, papillary response, deviation of gaze, extent of hemianopsia, facial palsy, resistance to gravity in the weaker limb, plantar reflexes, limb ataxia, sensory loss, visual neglect, dysarthria and aphasia severity.

Items are graded on a 3- or 4-point ordinal scale; 0 means no impairment. Scores range from 0 - 42. Higher scores indicate greater severity.

  1. Very Severe: >25
  2. Severe: 15 - 24
  3. Mild to Moderately Severe: 5 - 14
  4. Mild: 1 - 5
6 months
Stroke Specific Quality of Life Scale
Time Frame: 6 months

A quality of life measure designed for stroke subjects.

49 items Items are assessed on 5-point Guttman-type scales. Each item is answered using 1 of 3 different response sets.

Provides both summary and domain specific scores:

  1. Domain scores are composed of unweighted averages
  2. Summary scores are composed of an unweighted average of the 12 domain average scores Scores range from 49-245. Higher scores indicate better functioning.

The 12 domains include:

  1. Mobility
  2. Energy
  3. Upper Extremity Function
  4. Work and Productivity
  5. Mood
  6. Self-care
  7. Social Roles
  8. Family Roles
  9. Vision
  10. Language
  11. Thinking
  12. Personality
6 months
Healthcare utilization Questionnaire
Time Frame: 6 months
An informal questionnaire regarding unanticipated hospitalization, to be completed by participants at the end of the study.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 15, 2024

Primary Completion (Actual)

September 6, 2024

Study Completion (Actual)

September 6, 2024

Study Registration Dates

First Submitted

September 12, 2023

First Submitted That Met QC Criteria

September 27, 2023

First Posted (Actual)

October 4, 2023

Study Record Updates

Last Update Posted (Actual)

September 19, 2024

Last Update Submitted That Met QC Criteria

September 12, 2024

Last Verified

September 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

None will be shared

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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