KNA Proof-of-Concept
Primary Purpose
Adherence, Treatment, Retention, Cognitive Impairment, Mild
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Motivational Interviewing-Cognitive Behavioral Therapy Ketogenic Nutrition Adherence Program
Sponsored by

About this trial
This is an interventional prevention trial for Adherence, Treatment
Eligibility Criteria
Inclusion Criteria:
- Final inclusion criteria included individuals who met criteria for "possible" Mild cognitive impairment (MCI), which was defined as the following: evidence of either subjective decline in memory and greater self-reported use of compensatory strategies OR poorer performance than expected in one or more cognitive domain OR limited evidence of impairment in both subjective and objective findings.
Exclusion Criteria:
- Presence of severe and/or unstable medical conditions
- diagnosable major neurocognitive disorder
Sites / Locations
- Florida State University
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
MI-CBT KNA Program
Arm Description
6-week group intervention using MI and CBT strategies to promote adherence to a ketogenic nutrition program.
Outcomes
Primary Outcome Measures
Adherence
Assessed based on reported ketone levels during the program
Acceptability
Assessed based on qualitative feedback and online surveys
Retention
Assessed based on attendance and % of participants who remained in the program from start to finish
Secondary Outcome Measures
Cognitive functioning
Assessed using the Repeatable Battery for the Assessment of Neuropsychological Status - Update
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04968041
Brief Title
KNA Proof-of-Concept
Official Title
Feasibility Trial Assessing Adherence and Response to a Ketogenic Dietary Intervention for Individuals at High Risk for Alzheimer's Disease
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
September 27, 2019 (Actual)
Primary Completion Date
June 30, 2020 (Actual)
Study Completion Date
August 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Florida State University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The intervention program proof-of-concept was assessed as a single-arm, within-subjects clinical study with a target enrollment of 10 participants with possible or probable amnestic MCI. The protocol required participants to complete a pre-intervention assessment within two weeks of beginning the intervention, attend seven, one-hour intervention group sessions across six weeks, complete a post-assessment and interview in the final week of the intervention, and complete weekly surveys throughout the intervention.
Detailed Description
The primary goal of the proof-of-concept phase is to use pre-post comparisons to determine if the treatment package can produce clinically significant improvements. Thus, our goal was to assess whether the MI-CBT KNA program influenced adherence to KN and cognitive outcomes. Of note, recruitment for the trial occurred in the weeks leading up to the COVID-19 pandemic, which substantially altered the original intervention and assessment design due to restrictions on in-person human subject research. While the original protocol included in-person assessments and group meetings, collection of multiple biological samples (i.e., lipid panels, basic vitals, inflammatory biomarkers), and weekly health assessments, these in-person components were modified or removed for completion during the COVID-19 pandemic. Pre-assessment and screening appointments described below were completed in-person prior to the COVID-19 pandemic. Thus, we completed pre-intervention neuropsychological assessments with participants at baseline prior to beginning the trial; however, immediately following baseline assessments, we fully revised the protocol to include only online, video, and phone contact. We moved the KNA program to an online platform (HIPAA-compliant Zoom), and assessments were changed to online surveys and video assessments. Individual testing of the video platform was completed prior to the trial, which successfully reduced technical problems.
The MI-CBT KNA Program proof-of-concept was assessed as a single-arm, within-subjects clinical study with a target enrollment of 10 participants with possible or probable amnestic MCI. The protocol required participants to complete a pre-intervention assessment within two weeks of beginning the intervention, attend seven, one-hour intervention group sessions across six weeks, complete a post-assessment and interview in the final week of the intervention, and complete weekly surveys throughout the intervention. Participants were mailed materials, including the participant workbook and food, macronutrient, and ketone logs. Participants were also sent two bottles of ketone urine test strips for daily testing and materials to complete follow-up assessments. Throughout the program, participants were instructed to titrate into full ketosis across the first four weeks of the program by gradually reducing total carbohydrate intake and increasing healthy fat intake (e.g., fish, nuts, avocado, olive oils etc.). Thus, participants were not expected to attain measurable ketone levels until the final weeks of the program.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adherence, Treatment, Retention, Cognitive Impairment, Mild
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MI-CBT KNA Program
Arm Type
Experimental
Arm Description
6-week group intervention using MI and CBT strategies to promote adherence to a ketogenic nutrition program.
Intervention Type
Behavioral
Intervention Name(s)
Motivational Interviewing-Cognitive Behavioral Therapy Ketogenic Nutrition Adherence Program
Other Intervention Name(s)
MI-CBT KNA Program
Intervention Description
The intervention using strategies from motivational interviewing and cognitive behavioral therapy to promote motivation and adherence to ketogenic nutrition in older adults at high risk for Alzheimer's disease. The program is a 6-week, group program led by a psychologist and nutrition expert.
Primary Outcome Measure Information:
Title
Adherence
Description
Assessed based on reported ketone levels during the program
Time Frame
6-weeks
Title
Acceptability
Description
Assessed based on qualitative feedback and online surveys
Time Frame
6-weeks
Title
Retention
Description
Assessed based on attendance and % of participants who remained in the program from start to finish
Time Frame
baseline to 6-weeks
Secondary Outcome Measure Information:
Title
Cognitive functioning
Description
Assessed using the Repeatable Battery for the Assessment of Neuropsychological Status - Update
Time Frame
Baseline and 6-weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Final inclusion criteria included individuals who met criteria for "possible" Mild cognitive impairment (MCI), which was defined as the following: evidence of either subjective decline in memory and greater self-reported use of compensatory strategies OR poorer performance than expected in one or more cognitive domain OR limited evidence of impairment in both subjective and objective findings.
Exclusion Criteria:
Presence of severe and/or unstable medical conditions
diagnosable major neurocognitive disorder
Facility Information:
Facility Name
Florida State University
City
Tallahassee
State/Province
Florida
ZIP/Postal Code
32306
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35065656
Citation
Sheffler JL, Arjmandi B, Quinn J, Hajcak G, Vied C, Akhavan N, Naar S. Feasibility of an MI-CBT ketogenic adherence program for older adults with mild cognitive impairment. Pilot Feasibility Stud. 2022 Jan 22;8(1):16. doi: 10.1186/s40814-022-00970-z.
Results Reference
derived
Learn more about this trial
KNA Proof-of-Concept
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