Physical Activity Component of the Greek Interventional Geriatric Study to Prevent Cognitive Impairment and Disability (GINGER)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorUniversity of Patras

About this trial

The Greek Interventional Geriatric Study to Prevent Cognitive Impairment and Disability (GINGER) is a six-month multimodal, multicenter study aimed at people with Subjective Cognitive Impairement (SCI).

One of the GINGER's interventional components is the Physcial Activity (PA) component, coordinated by the University of Patras.

This PA component's scope is to determine whether an enhanced individualized physical exercise intervention programme can improve cognitive changes, physical function, quality of life and wellbeing in people with subjective cognitive decline.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Subjective Cognitive Decline confirmed from the Subjctive Cognitive Decline Questionnaire (SCD - Q score >7)

Absence of objective cognitive imparement as confirmed from cognitive assessment tests (i.e. MoCA, Trail A & B, Stroop, RCFT, FAS. )

Mild Cognitive Impairement (MCI) or dementia

Chronic psychiatric or neurological disorders affecting cognition (i.e. bipolar disorder, schizophrenia, MS, TBI, Parkinson's disease etc.)

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Physical Activity

    Behavioral

    The exercise programme is a 6-month progressive tailored-based exercise regime comprising * aerobic exercises (40-60%) * resistance exercises (20-40%) * balance with resistance exercises (20%) . This is peformed 3 times weekly, it is tailored to each individual but delivered in a small group-based manner. Two sessions are supervised by physiotherapist /exercise scientist and one session is unsupervised, home-based.

Treatment groups

200 Participants
are divided into 1 treatment group
Group A: Physical Activity interventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Balance

The Greek version of the Mini-BESTest (Mini-Balance Evaluation Systems Test) is used to assess the balance of each participant comprising four primary assessment balance categories (anticipatory, reactive postural control, sensory orientation, dynamic gait). The Mini-BESTest focuses primarily on dynamic balance and contains 14 different balancing tasks, each scored from 0 (lowest level of function) to 2 (highest level of function). Thus, overall scores range from 0 (lowest level of function) to 28 (highest level of function) and subsequent subscales are scored as: Anticipatory tasts (0-6), Reactive Postural Control (0-6), Sensory Orientation (0-6) \& Dynamic Gait (0-10). Mini-BESTest takes about 10-15 minutes to be administered.

Time frame
Baseline, midway (12-weeks), post-intervention (6months) & follow-up (3 months)
2

Upper limb muscle strength

The Hand Grip Strength test is an objective, established and standardised measure of upper limb muscle strength, comprising a standard electronic hand dynamometer (Jamar) for measuring muscle strength of the hand (measured in kgs).

Time frame
Baseline, midway (12-weeks), post-intervention (6months) & follow-up (3 months)
3

Lower limb muscle strength

The lower limbs strength is measured using the 30 seconds Sit-to-Stand test, which is an objective, established and standardised measure of lower limb muscle strength. Participants are seated in the front part of a standard chair with their hands crossed in front of their chest, and they are asked to stand up completely (full extension of their knees) and sit back down to the chair as many times as possible during 30 seconds (measuring the repetitions).

Time frame
Baseline, midway (12-weeks), post-intervention (6months) & follow-up (3 months)
4

Aerobic capacity

The 2 Minute Walk Test is an established and objective test for measuring aerobic capacity. Participants are placed in a hallway of nine meters and are asked to cover as much ground as they can in two minutes (measured in meters).

Time frame
Baseline, midway (12-weeks), post-intervention (6months) & follow-up (3 months)

Secondary outcomes

1

Fear of Falling

The Greek version of the Falls Self-efficacy International Scale (FES-I\_GREEK) is used to evaluate Fear of Falling. FES-I is a 16-item questionnaire with scores ranging from 16 to 64 points. Higher scores indicate higher fear and concern regarding falls.

Time frame
Baseline, midway (12-weeks), post-intervention (6months) & follow-up (3 months)
2

Physical Function

The International Physical Activity Questionnaire (IPAQ- 7) is used to evaluate physical function. IPAQ-7 is a 7-item questionnaire that calculates the physical activities taken place the last week (measured in METs).

Time frame
Baseline, midway (12-weeks), post-intervention (6months) & follow-up (3 months)
3

Adherance to exercise

The Exercise Adherance Rating Scale (EARS) is a validated and recently adapted into Greek outcome for measuring execise adhearance as well as the reasons of non-adhearing, comprising of 16 question items, exploring adhearance (6 question items) and reasons for adhearance/non-adhearance (10 items). Scores range from 0 (adherance) to 64 (non-adherance).

Time frame
Baseline, midway (12-weeks), post-intervention (6months) & follow-up (3 months)

Other outcomes

Sponsors and contacts

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University of Patras

Lead sponsor

University Hospital of Patras

Collaborator

University Hospital of Crete

Collaborator