← Back to Search

Behavioural Intervention

Telerehabilitation Experimental Group for Mild Cognitive Impairment (TCIFCF Trial)

N/A
Waitlist Available
Led By Grigore C Burdea, PhD
Research Sponsored by Bright Cloud International Corp
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline to 8 weeks and to 16 weeks from baseline
Awards & highlights

TCIFCF Trial Summary

This study is evaluating whether a computerized system can improve upper extremity motor and cognitive function in breast cancer survivors.

Eligible Conditions
  • Mild Cognitive Impairment

TCIFCF Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~screening at consent
This trial's timeline: 3 weeks for screening, Varies for treatment, and screening at consent for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Brief Visuo-spatial Memory Test, Revised (BVMT-R)
Change in Hopkins Verbal Learning Test Revised
Change in Montreal Cognitive Assessment (MoCA)
+4 more
Secondary outcome measures
Caregiver Quality of Life-Cancer (CQOL-C)
Change in Beck Depression Inventory II
Change in Chedokee test (CAHAI-9)
+9 more
Other outcome measures
Change in Blood pressure (systolic and diastolic)
Change in Heart rate
Cyber-sickness Susceptibility Questionnaire for participant

TCIFCF Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Telerehabilitation experimental groupExperimental Treatment1 Intervention
Experimental training will occur in the home. The experimental training will last 8 weeks, each week having up to 4 sessions of therapeutic game play (based on tolerance). Each session will start with vitals being measured and logged. Data will be uploaded on a secure cloud server to which clinicians will have access.
Group II: Telerehabilitation control groupPlacebo Group1 Intervention
Participants will perform web-based game play while wearing sham equipment. Duration of sessions will be fixed and frequency of sessions will equal that of the experimental group training. Over the total training the control group will have an equal duration of training with the experimental group.

Find a Location

Who is running the clinical trial?

Bright Cloud International CorpLead Sponsor
7 Previous Clinical Trials
60 Total Patients Enrolled
National Cancer Institute (NCI)NIH
13,667 Previous Clinical Trials
40,926,126 Total Patients Enrolled
Rutgers, The State University of New JerseyOTHER
429 Previous Clinical Trials
64,192 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Telerehabilitation Cognitive Impairments Following Chemotherapy Feasibility Study
2022. "Telerehabilitation Cognitive Impairments Following Chemotherapy Feasibility Study". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04972019.
~13 spots leftby Apr 2025
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Back to top