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NCT Number: NCT06525987

Telecoached Exercise Intervention for Connectivity Enhancement in Small Vessel Disease (TELECONNECT-SVD)

The TELECONNECT-SVD study is a prospective, randomized, multicenter trial aimed at testing the efficacy of a remotely delivered exercise protocol on brain functional connectivity in patients with small vessel disease (SVD)-related ischemic stroke. The study will recruit patients aged ≥60 with a history of lacunar stroke, minimal disability (modified Rankin Scale score 0-1), and low physical activity levels.

The trial will include 60 participants randomized 1:1 to either a 24-week telecoached exercise intervention or usual care. The exercise program consists of multicomponent physical exercises delivered remotely twice a week. Assessments will be conducted at baseline, 12 weeks, 24 weeks, and 48 weeks.

Primary outcomes include changes in brain functional connectivity assessed by high-density EEG and improvements in physical fitness measured by the Senior Fitness Test. Secondary outcomes encompass changes in physical activity levels, anthropometric measurements, and vital signs.

The study employs a "wait list" design, where the control group receives the intervention after the initial 24-week period. This approach allows for assessment of the intervention's immediate effects and the retention of benefits after cessation.

Key features of the protocol include:

* Use of telecoaching to enhance adherence to the exercise program * Comprehensive assessment of brain connectivity using advanced EEG analysis techniques * Focus on patients with SVD, who may benefit significantly from exercise interventions * Evaluation of both neurophysiological and clinical outcomes

The study aims to provide evidence for the potential benefits of exercise in enhancing brain connectivity and physical fitness in SVD patients, potentially informing future treatment guidelines and preventive strategies for this population.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UOC Neurologia e Stroke Unit

Avezzano, L'Aquila, 67051, Italy

Location status: Recruiting

Location contact

Raffaele Ornello, MD, PhD

CONTACT

[email protected]

+390863499322

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥60 years;
  • History of lacunar stroke occurred between 3 months and 10 years from screening and confirmed by neuroimaging or clinical data by an expert stroke physician;
  • Modified Rankin Scale (mRS) score of 0-1, indicating no symptoms or no significant disability;
  • A level of physical activity below recommended targets, i.e. <150 minutes per week of moderate-to-vigorous exercise (24);
  • Ability to sign informed consent.

Exclusion criteria

  • Uncontrolled hypertension;
  • Heart disease impairing the possibility of safely following an exercise protocol at the discretion of the treating physician;
  • Primary or secondary epilepsy;
  • Prostheses, implants, and any device that might impair the performance of either high-density electroencephalogram or the exercise intervention;
  • Cognitive impairment (Mini Mental State Examination score ≤26 at follow-up);
  • Lack of access to Internet-based facilities or poor technological alphabetization impairing the adherence to the trial protocol;
  • Any major physical or psychiatric comorbidity that in the judgement of the treating physician might compromise the ability to undergo an exercise intervention.

Treatment and study plan

Physical activity

Behavioral

Randomization to a 24-week physical exercise program

Other names: Physical activity (delayed)

Primary outcomes

  1. Change in Senior Fitness Test score

    Time frame: 24 weeks

    Change in the Senior Fitness score from before to after the 24-week physical exercise intervention

Secondary outcomes

  1. Change in International Physical Activity Questionnaire (IPAQ) score

    Time frame: 24 weeks

    Change in International Physical Activity Questionnaire (IPAQ) score from before to after the 24-week physical exercise intervention

  2. Change in Body Mass Index

    Time frame: 24 weeks

    Change in Body Mass Index score from before to after the 24-week physical exercise intervention

  3. Change in blood pressure

    Time frame: 24 weeks

    Change in blood pressure from before to after the 24-week physical exercise intervention

  4. Change in heart rate

    Time frame: 24 weeks

    Change in heart rate from before to after the 24-week physical exercise intervention

Other outcomes

  1. Change in brain functional connectivity

    Time frame: 24 weeks

    Overall brain functional connectivity in the resting state assessed via high-density electroencephalogram

Study contacts

Contact information is provided by the study sponsor or research team.

Raffaele Ornello, MD, PhD

CONTACT

[email protected]

+390863499322

Sponsors and collaborators

Lead sponsor

University of L'Aquila

Other

Collaborators

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Registry information

Official study title

Telecoached Exercise Intervention for Connectivity Enhancement in Small Vessel Disease (TELECONNECT-SVD): a Randomized Clinical Trial

Acronym: TELECONNECT

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 29, 2024
Registry last updated
Dec 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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