CIRCuiTS MS: Improving Cognitive Recovery in Multiple Sclerosis

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to find out whether an adapted version of an existing cognitive rehabilitation program, CIRCuiTS (https://www.circuitstherapyinfo.com), can be used to improve everyday thinking skills for people with Multiple Sclerosis (MS). People living with MS have worked with the study's researchers to adapt CIRCuiTS to meet their needs. They shared the thinking challenges they experience and suggested changes to the program's content and how it is delivered. This study will test whether this adapted version can be delivered practically to people with MS in a trial setting and explore its potential benefits. The findings will help plan a larger trial testing how effective CIRCuiTS is in helping people with MS. Twenty-four people with MS will take part in this pilot trial. Each person will be randomly assigned to start the program either right away or after a 13-week wait. The therapy program involves up to 36 hours of therapist-led and independent sessions over 12 weeks in which the participant builds thinking skills through developing personal strategies for carrying out digital versions of tasks they find challenging. The practicality of delivering the program to people with MS will be judged based on whether problems arise in the trial, such as not being able to recruit enough people or participants not liking it. To explore its potential benefits, the study will check for improvements in progress toward personal goals, thinking abilities, emotional well-being, chronic tiredness, and daily living skills after the therapy. If delivering CIRCuiTS to people with MS is found to be both practical and acceptable to participants, the findings of this trial will be used to design a larger-scale trial of its effectiveness. Ultimately, the goal of this project is to improve the quality of life of people living with cognitive difficulties related to MS.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants must have a confirmed diagnosis of Multiple Sclerosis (MS), as verified by a healthcare provider.

• Participants should be in a relatively stable phase of their condition, not experiencing a severe relapse or acute health crisis at the time of the study.

• Participants must have sufficient cognitive abilities to engage in therapy sessions, meaning they can follow instructions and perform the cognitive tasks required during the remediation program.

• Participants must be able to effectively communicate in English, both verbally and in writing, to interact with therapists and complete assessments.

• Participants must be adults aged 18 years or older.

• Participants should have personal experience with cognitive challenges related to MS, such as problems with memory, attention, or problem-solving.

• Participants must be willing and able to commit to attending all therapy sessions over the 12-week period, as well as attending assessments and completing any required homework or independent sessions.

• Participants must provide informed consent, demonstrating that they understand the purpose of the therapy trial and are willing to engage in the course of cognitive remediation.

• Participants must have access to a computer (laptop or desktop) for at least one hour per week during the treatment period (12 weeks).

Locations
Other Locations
United Kingdom
King's College London
RECRUITING
London
Contact Information
Primary
Rebecca Thomas, PhD
Rebecca.j.thomas@kcl.ac.uk
+44 2078485633
Backup
Matteo Cella, PhD
matteo.cella@kcl.ac.uk
+44 20 7848 5001
Time Frame
Start Date: 2025-07-17
Estimated Completion Date: 2026-09-15
Participants
Target number of participants: 24
Treatments
Experimental: Immediate Treatment Group
Participants will start the cognitive remediation program immediately after recruitment. Outcome measures will be taken before treatment (week 1), immediately after treatment (week 14), and at 14 weeks after end of treatment (week 27).
Experimental: Delayed Treatment Group
Participants will start the cognitive remediation program after being on a waitlist for 13 weeks. Outcome measures will be taken when added to the waitlist (week 1), before treatment (week 14), and immediately after treatment (week 27).
Related Therapeutic Areas
Sponsors
Collaborators: King's College Hospital NHS Trust
Leads: King's College London

This content was sourced from clinicaltrials.gov