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Tailored Mediterranean Lifestyle Education in Participants With Subjective Cognitive Impairment

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03569319
Enrollment
5
Registered
2018-06-26
Start date
2018-05-18
Completion date
2019-06-30
Last updated
2024-04-03

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

Conditions

Subjective Cognitive Impairment

Keywords

Mediterranean Diet, Lifestyle

Brief summary

It is estimated that 30% of Alzheimer's disease cases globally are associated with changeable risk factors, such as diet and physical activity. In particular, a Mediterranean diet (MD) has been associated with reduced risk of cognitive decline and improved brain function. The investigators developed educational resources on the Mediterranean diet and lifestyle (THINK-MED) in accordance with the Medical Research Council guidance for developing and evaluating complex interventions, based on a systematic literature review and informed by qualitative work with patients with mild memory problems.The feedback gathered informed refinements and tailoring of the resource and overall MD intervention. This study aims to evaluate feasibility of the THINK-MED Mediterranean lifestyle educational intervention to encourage dietary behaviour change among community-dwelling people with subjective cognitive impairment.

Detailed description

This pilot RCT aims to evaluate the feasibility of a theory-based, tailored Mediterranean lifestyle education intervention (THINK-MED) to encourage behaviour change among participants who have subjective cognitive impairment. This study will be a 6 month randomised controlled trial (RCT) with a total of 30 participants who will be randomised to 1 of 3 groups: 1. Group 1 will receive the THINK-MED Mediterranean Lifestyle Education for Memory resource on one occasion at baseline (n=10) 2. Group 2 will receive the THINK-MED Mediterranean Lifestyle Education for Memory resource at monthly intervals for 5 months, with an initial face-to-face visit from the research dietitian (month 1) and accompanied by telephone feedback (month 2-5) (n=10) 3. Group 3 is a control group. Participants in this group will receive the THINK-MED Mediterranean Lifestyle Education for Memory resource after completing the 6 month study (n=10)

Interventions

BEHAVIORALTHINK-MED resource (baseline)

The THINK-MED 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.

BEHAVIORALTHINK-MED resource (staged)

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

BEHAVIORALControl

Participants will receive the THINK-MED resource after their final 6 month study visit (i.e. delayed intervention).

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

* Have subjective cognitive impairment - Montreal Cognitive Assessment (MoCA) score ≥ 26/30 * Mediterranean diet score (MDS) ≤ 4 (Estruch et al. 2006) * Willing to make changes to their diet

Exclusion criteria

* Diagnosis of dementia * MoCA score of ≤ 25/30 * Individuals with a visual or English language impairment * Psychiatric problems e.g. depression * Significant medical comorbidity * Body Mass Index (BMI) ≤ 19 and ≥ 40 kg/m2 * Excessive alcohol consumption * 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 with a increase in score by greater than or equal to 3 points at 6 months indicating adoption (maximum score 14)

Secondary

MeasureTime frameDescription
4 day food diaryBaseline, 6 monthsA food diary will be completed to assess compliance with a Mediterranean diet
Mediterranean Diet self-efficacy questionnaireBaseline, 6 monthsA questionnaire to measure participants self-efficacy
Barriers to consuming a Mediterranean Diet questionnaireBaseline, 6 monthsDietary behaviour change questionnaire to measure adherence to a Mediterranean diet
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.
Change in Physical Activity at 6 monthsBaseline, 6 monthsPhysical activity will be measured by the Recent Physical Activity Questionnaire (RPAQ)
Anthropometric measurementsBaseline, 6 monthsWeight and height measurements to calculate BMI
Muscle StrengthBaseline, 6 monthsMeasured using a grip-strength dynamometer
Geriatric Depression ScaleBaseline, 6 monthsDepressive symptoms will be measured by the Geriatric Depression Scale Questionnaire, with a score greater than 5 indicating depressive symptoms
Functional Assessment (1)Baseline, 6 monthsMeasured by the instrumental activities of daily living questionnaire (IADL) by Lawton and Brody Measured by the instrumental activities of daily living scale (IADL) by Lawton and Brody (1969) questionnaire
Functional Assessment (2)Baseline, 6 monthsMeasured by the Bristol activities of daily living (Bucks et al. 1996) 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.)
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 Short Form-36 HEALTH SURVEYBaseline, 6 monthsA questionnaire to measure participants views and beliefs on health
Staging Algorithm QuestionnaireBaseline, 6 monthsA questionnaire to measure participants readiness to change their diet and lifestyle

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