The effect of flicker stimulation of peripheral visual field on short-term recall.

ISRCTN ISRCTN35316120
DOI https://doi.org/10.1186/ISRCTN35316120
Protocol serial number N0176135497
Sponsor Department of Health
Funder Oxford Radcliffe Hospitals NHS Trust (UK)
Submission date
30/09/2004
Registration date
30/09/2004
Last edited
14/07/2009
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Signs and Symptoms
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr Jonathan Williams
Scientific

OPTIMA
Radcliffe Infirmary
Woodstock Road
Oxford
OX2 6HE
United Kingdom

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Scientific title
Study objectivesTo test if flicker can enhance short-term recall in older people. To test if any flicker effects on short term recall are frequently-specific.
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedSigns and Symptoms: Memory
InterventionRandomised trial. The intervention is learning and recall of words. A flicker machine will occur on light emitting diodes, the randomisation will be the flicker frequencies. It is thought that specific frequencies (near 10Hz) will enhance recognition and lower and higher frequencies will not.
Intervention typeOther
Primary outcome measure(s)

The endpoints of the study will be recognition of words that participants saw during the learning phase. We will test if particular frequencies of flicker that occurred in the learning phase enhance recognition.

Key secondary outcome measure(s)

Not provided at time of registration

Completion date28/02/2005

Eligibility

Participant type(s)Patient
Age groupSenior
SexAll
Target sample size at registration100
Key inclusion criteria50 healthy people, 50 patients
Key exclusion criteriaDoes not match inclusion criteria
Date of first enrolment19/12/2003
Date of final enrolment28/02/2005

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

OPTIMA
Oxford
OX2 6HE
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 05/03/2006 Yes No