Skip to content

Tailored Mediterranean Lifestyle Education in Patients With Mild Cognitive Impairment

The Development and Pilot Testing of Tailored Mediterranean Lifestyle Education to Encourage Behaviour Change in Patients With Mild Cognitive Impairment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03265522
Enrollment
15
Registered
2017-08-29
Start date
2017-05-01
Completion date
2019-06-30
Last updated
2019-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Impairment

Keywords

Mediterranean diet, Lifestyle

Brief summary

Evidence suggests that a Mediterranean diet can have a beneficial effect on brain health. Mild cognitive impairment (MCI) describes problems with brain function such as difficulty with day-to-day memory and concentration. It is at this stage that Mediterranean diet could prove beneficial in terms of prevention. Previous research by Queens University investigated the opinions of patients with MCI and their care givers to inform the development of Mediterranean diet education material to encourage behaviour change. The study suggested that MCI patients lacked awareness of the link between Mediterranean diet and brain function, although were interested to learn more. Feedback on the developed educational material was positive although there were suggested improvements such as tailoring information to memory loss, a potential staged approach to delivery and adaptations to the material content. This present study aims to pilot test refined educational material among MCI participants to evaluate the feasibility of encouraging dietary behaviour change among this patient group.

Detailed description

This study aims to evaluate the feasibility of a theory-based, tailored Mediterranean lifestyle education intervention to encourage behaviour change in patients with MCI. The proposed study will be a 6 month RCT with a total of 60 MCI patients who will be randomised to 1 of 3 groups: 1. Group 1 will receive the Mediterranean lifestyle education resource on one occasion at baseline 2. Group 2 will receive the Mediterranean lifestyle education resource at monthly intervals for 5 months accompanied by telephone feedback from the research dietitian 3. Group 3 will receive standard care (control group). Participants will receive the Mediterranean lifestyle education resource after their final 6 month study visit (i.e. delayed intervention).

Interventions

BEHAVIORALThinkMed resource at baseline

The ThinkMed resource contains an information booklet, recipe books, menu plan cards, shopping list cards and goal setting cards. Participants will receive this resource on one occasion at baseline.

Participants will continue with the standard care provided by their physician. Participants will receive the ThinkMed resource after their final 6 month study visit (i.e. delayed intervention).

BEHAVIORALThinkMed resource (staged)

This group of participants will receive the ThinkMed resource at monthly intervals for 5 months accompanied by telephone feedback from the research dietitian

Sponsors

Wellcome Trust
CollaboratorOTHER
Queen's University, Belfast
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Mild Cognitive Impairment by their physician * Mediterranean diet score (MDS) less than or equal to 4 (Estruch et al., 2006) * Willing to make changes to their diet

Exclusion criteria

* Diagnosis of dementia * Patients with visual or English language impairment * Psychiatric problems * Significant medical comorbidity * Body Mass Index (BMI) ≤ 19 and ≥ 40 kg/m2 * Excessive alcohol consumption * Taking high dose nutritional supplements * Dietary restrictions/allergies that would substantially limit ability to complete study requirements * Inability to provide informed consent * History of, or comorbid condition which may alter performance on cognitive tests e.g. stroke, head injury, Parkinson's disease, learning disability

Design outcomes

Primary

MeasureTime frameDescription
Change in Mediterranean Diet Score (MDS) at 6 monthsBaseline, 6 monthsMediterranean dietary intake will be measured by a validated questionnaire

Secondary

MeasureTime frameDescription
Blood SampleBaseline, 6 monthsA blood sample will be taken from participants to be stored for analysis of biomarkers of MD adherence and biomarkers of neurodegenerative disease risk.
Staging Algorithm QuestionnaireBaseline, 6 monthsA questionnaire to measure participants readiness to change their diet and lifestyle
Mediterranean Diet self-efficacy questionnaireBaseline, 6 monthsA questionnaire to measure participants self-efficacy
Mediterranean diet tolerance questionnaireBaseline, 6 monthsA questionnaire to measure tolerance to a Mediterranean diet
Physical ActivityBaseline, 6 monthsRPAQ-Recent Physical Activity Questionnaire
Anthropometric measurementsBaseline, 6 monthsWeight and height measurements to calculate BMI
Muscle StrengthBaseline, 6 monthsMeasured using a grip-strength dynamometer
Geriatric Depression ScaleBaseline, 6 monthsGeriatric Depression Scale Questionnaire
Functional Assessment (1)Baseline, 6 monthsMeasured by the instrumental activities of daily living scale (IADL) by Lawton and Brody (1969) questionnaire
Cognitive AssessmentBaseline, 6 monthsA comprehensive cognitive assessment will be performed, including: global cognition, motor skills, executive function episodic/visual memory, and information processing and sustained attention using a validated neuropsychological test battery (Cantab Cognitive Battery, Cambridge Cognition Ltd.)
Barriers to consuming a Mediterranean Diet questionnaireBaseline, 6 monthsDietary behaviour change questionnaire to measure adherence to a Mediterranean diet
Functional Assessment (2)Baseline, 6 monthsMeasured by the Bristol activities of daily living scale (Bucks et al. 1996) questionnaire
4-day Food DiaryBaseline, 6 monthsA food diary will be completed to assess compliance with a Mediterranean diet
Change in Lifestyle questionnaireBaseline, 6 monthsA questionnaire to measure change in lifestyle behaviours
Dietary Quality of Life questionnaireBaseline, 6 monthsA questionnaire to measure dietary quality of life
Mediterranean Diet Knowledge questionnaireBaseline, 6 monthsA questionnaire to measure participants Mediterranean diet knowledge
Rand SF-36 HEALTH SURVEYBaseline, 6 monthsA questionnaire to measure participants views and beliefs on health

Other

MeasureTime frameDescription
Process Evaluation (3) - structured interviewsup to 3 months post interventionPost intervention structured interviews for participant evaluation of the intervention programme and dietary educational materials
Process Evaluation (2) - study recordsup to 3 months post interventionA review of study records- including attrition rates, reason for dropout
Process Evaluation (1) - telephone contact evaluationup to 3 months post interventionDetermination individual participation and engagement with the intervention by reviewing telephone contact log record and telephone checklist evaluation

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026