NCT01603862

Brief Summary

Dementia is serious problem and around 700 000 people are affected in the UK alone. Currently there is no cure however early diagnosis and effective treatment offers hope for reducing the impact. Dementia sufferers require care due to physical disability, cognitive deficits, social isolation and emotional symptoms (depression). Delaying the onset of dementia will improve quality of life for patients and reduce the cost of residential care (£42 000 per person per year). People with mild cognitive impairment (MCI) are at high risk of developing dementia. They have impaired cognitive abilities, such as memory, but still manage their everyday activities. Studies show that 8 out of 10 people with MCI will have developed dementia 6 years after diagnosis. Regular physical activities and performing a variety of cognitive activities reduce the risk of dementia and improves abilities and quality of life in healthy people. Therefore a combination of these activities may reduce the risk of developing dementia in MCI. The investigators want to see if they can develop a program which combines these activities in a fun and social way that gets people active and keeps them active. The aims are to improve fitness, cognition and quality of life. The investigators plan to use computers and the internet to help with the activities and to make them available to people who are isolated. Physical activity will involve walking from home, cognitive activities will be computer based games and puzzles and socialising will involve regular varied group-based activities. Participants (128) will be recruited from the UCL Derwent Memory Clinic and will complete a 26 week program. They will then be followed up yearly to monitor their progress. The main outcome of the study is engagement in the activities. The investigators will also measure fitness, cognition, quality of life and conversion to dementia.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
128

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2010

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2010

Completed
2.4 years until next milestone

First Submitted

Initial submission to the registry

May 17, 2012

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 23, 2012

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2012

Completed
Last Updated

April 28, 2014

Status Verified

April 1, 2014

Enrollment Period

2.8 years

First QC Date

May 17, 2012

Last Update Submit

April 25, 2014

Conditions

Outcome Measures

Primary Outcomes (1)

  • Activity Compliance

    Number of participants to have completed 50% or more of the programmed activity sessions during the intervention period.

    Compliance with programmed activities will be assessed at the end of participation which is expected to be at 24 weeks

Secondary Outcomes (3)

  • Cardiovascular fitness measure

    This will be measured at the start, after the control period (12 weeks) and after completion of the activity interventions at around 24 weeks.

  • Cognitive measures

    This will be measured at the start, after the control period (12 weeks) and after completion of the activity interventions at around 24 weeks.

  • Measures of quality of life and everyday activities

    This will be measured at the start, after the control period (12 weeks) and after completion of the activity interventions at around 24 weeks.

Study Arms (1)

ThinkingFit

EXPERIMENTAL
Procedure: ThinkingFit programme

Interventions

Combined physical, cognitive and social stimulation activties.

ThinkingFit

Eligibility Criteria

Age40 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients fulfilling criteria for AMCI \[Petersen et al. 2001b\]:
  • i. Memory impairment for age and education ii. No impairment in other cognitive domains iii. Normal social activities iv. Patient is not demented
  • For the other subtypes of MCI, cognitive impairment in one or more nonmemory domain
  • Sedentary lifestyle with no regular participation in physical exercise defined as two or three times a week for at least 20 minutes duration, or participation in active sport more than once a week, in the previous six months.
  • Willing and able to give informed consent.
  • Availability and access to safe exercise environments, such as paths or roads with sidewalks for walking or cycling.
  • At low risk from serious adverse effects from increased physical activity as indicated by performance on the revised Physical activity readiness questionnaire (PARQ).

You may not qualify if:

  • Type 1 (insulin dependent) diabetes mellitus.
  • Blood pressure of 160/100 mmHg or more.
  • Body weight more than 140% of ideal body weight.
  • Musculoskeletal or other medical problems preventing safe participation in regular moderate intensity exercise (65-77% of predicted maximum heart rate). This will include a resting tachycardia (heart rate above 100 bpm) and history of myocardial infarction or unstable angina within the last month.
  • Participants taking medications affecting heart rate will need to be on a stable dosing regime for 3 months prior to commencing in order to control for potential spurious results on fitness measures caused by these treatments.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

North Essex Partnership Foundation NHS Trust

Harlow, Essex, cm20 1qx, United Kingdom

Location

Related Publications (1)

  • Dannhauser TM, Cleverley M, Whitfield TJ, Fletcher BC, Stevens T, Walker Z. A complex multimodal activity intervention to reduce the risk of dementia in mild cognitive impairment--ThinkingFit: pilot and feasibility study for a randomized controlled trial. BMC Psychiatry. 2014 May 5;14:129. doi: 10.1186/1471-244X-14-129.

MeSH Terms

Conditions

Cognitive Dysfunction

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental Disorders

Study Officials

  • Martin Cleverley

    North Essex Partnership Foundation NHS Trust

    PRINCIPAL INVESTIGATOR
  • Thomas M Dannhauser, PhD

    University College London, North Essex Partnership NHS Foundation Trust

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Consultant Psychiatrist and Honorary Senior Lecturer in Psychiatry

Study Record Dates

First Submitted

May 17, 2012

First Posted

May 23, 2012

Study Start

January 1, 2010

Primary Completion

November 1, 2012

Study Completion

November 1, 2012

Last Updated

April 28, 2014

Record last verified: 2014-04

Locations