A Modified Test of Goal-directed Behaviour: a Feasibility Study
Feasibility Study for Development of a Modified Bedside Test of Goal-directed Behaviour
2 other identifiers
interventional
30
1 country
2
Brief Summary
Cognitive assessment plays an important part in decision making in acute neurological settings, partly because difficulties with cognitive skills such as attention, memory and executive functioning (which includes planning and problem-solving) have direct implications for patents' levels of independence and safety upon discharge. A bedside cognitive task that could shed light upon a patient's ability to demonstrate effective goal-directed behaviour (potentially along with other aspects of executive functioning such as cognitive flexibility) would be a useful addition to the existing repertoire of bedside cognitive assessments. One such test could be 'Link's Cube'. The Link's Cube Test is impractical for bedside use in an acute ward setting, as it comprises 27 small blocks. The feasibility study aims to preserve the information that is provided by Link's Cube Test (i.e. an indication of the patient's ability to engage in goal-directed behaviour) whilst altering the testing material such that only nine, slightly larger blocks are used. The objectives for the feasibility study are:
- To identify any practical difficulties in administration of the tests that may not be apparent without trialling them
- To generate information regarding the timing and sequence of overall administration and in particular the proposed modified Link's Cube test
- To obtain feedback from neuropsychologists about ease of administration of the proposed new test and to obtain their views regarding potential benefits
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2025
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 15, 2025
CompletedFirst Submitted
Initial submission to the registry
January 29, 2026
CompletedFirst Posted
Study publicly available on registry
March 19, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedApril 27, 2026
April 1, 2026
7 months
January 29, 2026
April 24, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Procedural obstacles of the modified Link's Cube test.
Assessed using the Link's Cube Scoring Matrix (total score between 0-30)
Day 1
Study Arms (2)
Neuropsychologists
OTHERClinical psychologists in Gloucestershire Hospitals NHS FT
Non-neuropsychologists
OTHERGeneral population, non-neuropsychologists
Interventions
The five tests are: * Link's Cube: participants are asked to construct a large cube from 27 smaller cubes such that the outer surface is all the same colour * Modified Links' Cube: participants are asked to construct a large cube from 9 smaller blocks such that the outer surface is all the same colour, and then amend their response according to 2 further instructions * D-KEFS Tower Test - participants are asked to move discs of varying sizes across three pegs to build a target tower in as few moves as possible * Weigl test - participants are asked to sort blocks into one group according to shape/colour and then shift mental set by sorting them according to the second characteristic * Brixton Spatial Anticipation test - participants are asked to detect rules and rule changes when presented a targets that changes location
Eligibility Criteria
You may qualify if:
- General population. For convenience at this feasibility study stage this will be largely comprised of colleagues working with GHT, above the age of 18, with no upper age limit.
- Have given informed consent having followed the procedure in the protocol
- Have the physical/sensory abilities to undertake the test procedures (e.g. use of both hands, adequate vision)
- Sufficient English language to be able to follow test instructions
You may not qualify if:
- Under the age of 18
- Refusal/inability to give informed consent
- Insufficient English language to be able to follow test instructions
- Using cognitive testing as part of their clinical work, or ongoing familiarity with cognitive tests.
- Working directly with the main investigator.
- Presence of a self-reported cognitive difficulty/neurological condition - not because that in itself would be problematic for test administration or for the information generated, but rather to avoid potential distress to participants were they to find the tests administered challenging.
- Presence of any physical/sensory/cognitive difficulty that would confound administration of the tasks, e.g. being partially sighted or having use of only one upper limb
- clinical psychologists in GHT who have or have had a role that involves the administration of cognitive tests
- Have given informed consent having followed the procedure in the protocol
- Have the physical/sensory abilities to undertake the test procedures (e.g. use of both hands, adequate vision)
- Sufficient English language to be able to follow test instructions
- Under the age of 18
- Refusal/inability to give informed consent
- Insufficient English language to be able to follow test instructions
- Presence of a self-reported cognitive difficulty/neurological condition - not because that in itself would be problematic for test administration or for the information generated, but rather to avoid potential distress to participants were they to find the tests administered challenging.
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Cheltenham General Hospital
Cheltenham, Gloucestershire, GL53 7AN, United Kingdom
Gloucestershire Royal Hospital
Gloucester, Gloucestershire, GL1 3NN, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 29, 2026
First Posted
March 19, 2026
Study Start
September 15, 2025
Primary Completion
April 1, 2026
Study Completion
April 1, 2026
Last Updated
April 27, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share