FORGET: Reshaping the Motor Engram - An Online Crowdsourcing Study.

Sponsor
Medical University of South Carolina (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05511480
Collaborator
National Institute of General Medical Sciences (NIGMS) (NIH)
412
1
4
4.5
90.9

Study Details

Study Description

Brief Summary

A critical point in learning and memory research is whether memories, once consolidated, remain unchanged or whether they continue to undergo plastic changes and remodeling. While previous research has focused on experimental destabilization during early stages of the memory life cycle, i.e., during encoding or early consolidation, experimental data that provides information about the effect of destabilization interventions on well-consolidated memories is still missing. This is particularly true for the procedural memory domain, such as learning a sensorimotor skill. This project is designed to characterize the effect of a single behavioral interference intervention on a previously consolidated sensorimotor skill in a large sample of healthy volunteers recruited through an online crowdsourcing platform. In a longitudinal design, participants will perform an implicit sequence learning task over five consecutive sessions, followed by an interference intervention in session six and a follow-up evaluation of the stability of the learned skill in session seven. The experimental design includes two levels of sequential information (spatial and temporal), which allows the testing of the specificity of the interference intervention. Behavioral performance throughout the experimental sessions is acquired via the manual input on the participants' computer keyboards and used to extract the learning rate and the interference effect (primary outcome).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Interference through learning of a competing motor skill.
  • Behavioral: No interference
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
412 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Basic Science
Official Title:
Reshaping the Motor Engram - An Online Crowdsourcing Study.
Anticipated Study Start Date :
Aug 15, 2022
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Interference on sequence 1

The interference intervention (session six) will be applied to one of the two previously learned sequences (temporal).

Behavioral: Interference through learning of a competing motor skill.
Interference through the learning of a competing motor skill.

Experimental: Interference on sequence 2

The interference intervention (session six) will be applied to one of the two previously learned sequences (spatial).

Behavioral: Interference through learning of a competing motor skill.
Interference through the learning of a competing motor skill.

Experimental: Interference on sequences 1 and 2

The interference intervention (session six) will be applied to both of the two previously learned sequences (temporal and spatial).

Behavioral: Interference through learning of a competing motor skill.
Interference through the learning of a competing motor skill.

Sham Comparator: No interference

The interference intervention (session six) will be applied.

Behavioral: No interference
No interference through the continuation of learning same motor skill

Outcome Measures

Primary Outcome Measures

  1. Immediate interference rate (change in performance precision) [six days]

    Performance in the learning task is derived from the precision of timing of key presses relative to the occurrence and duration of visual cues presented on the computer screen. The interference rate is operationalized as the change in performance precision over time. The immediate interference effect is analyzed based on the change in performance from before (pre-interference) the interference intervention to directly after the interference intervention in session six (post-interference). This change is normalized to the performance at baseline (pre-interference session six) and computed as [(post-interference - pre-interference)/pre-interference*100].

  2. Delayed interference rate (change in performance precision) [seven days]

    The delayed interference rate is calculated in analogy to the immediate interference effects with a 24-hours latency of the post-interference measure. Delayed interference is analyzed based on the change in performance from before the interference intervention (pre-interference in session six) to 24 hours after the interference intervention in session seven (24hours post-interference). This change is normalized to the performance at baseline (pre-interference session six) and computed as [(24 hours post-interference - pre-interference)/pre-interference*100].

Secondary Outcome Measures

  1. Learning rate (change in performance precision) [five days]

    Skill learning is defined based on the precision of timing of key presses relative to the occurrence and duration of visual cues presented on the computer screen. Skill learning is indexed by increased precision over time, operationalized as declining deviation of key on- and offsets from the timing of cue on- and offsets. Learning rate is the absolute change of precision over the learning phase of five days, which is expected to follow an asymptotic exponential function.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • registered Amazon Mechanical Turk users (called 'workers')

  • with >95% approval rate on all previous Amazon Mechanical Turk assignments

  • location in North America or Europe

  • ≥18 years of age

  • not having participated in this experiment before

Exclusion Criteria:

• prior participation in this experiment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of South Carolina Charleston South Carolina United States 29425

Sponsors and Collaborators

  • Medical University of South Carolina
  • National Institute of General Medical Sciences (NIGMS)

Investigators

  • Principal Investigator: Kirstin-Friederike Heise, PhD, Medical University of South Carolina

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kirstin-Friederike Heise, PhD, Assistant Professor, Medical University of South Carolina
ClinicalTrials.gov Identifier:
NCT05511480
Other Study ID Numbers:
  • 00118731
  • U54GM104941
First Posted:
Aug 23, 2022
Last Update Posted:
Aug 23, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 23, 2022