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Evaluation of a Home-based AOMI Intervention on Cognitive Function and Depression Among Adults with SCI

NCT06708026 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2025-02-06

No results posted yet for this study

Summary

The investigators propose a pilot randomized clinical trial to determine if adults with spinal cord injury (SCI) show improved cognitive function and depression following home-based Action Observation and Motor Imagery (AOMI) training. It is hypothesized that the home-based AOMI intervention will show satisfactory feasibility and acceptability. They also hypothesize that AOMI training can be used as a rehabilitative tool for improving cognitive function and depression in adults with SCI, because it engages and strengthens similar neural systems as actual exercise.

Conditions

  • Spinal Cord Injuries (SCI)
  • Depression
  • Motor Imagery
  • Cognitive Functions

Interventions

BEHAVIORAL

Action Observation and Motor Imagery (AOMI) training

Participants will watch home-based exercise videos and simultaneously imagine themselves performing these exercises in their minds by following verbal instructions in the videos, without actual execution.

BEHAVIORAL

Basic wheelchair exercises

A set of low-intensity warm-up wheelchair exercises developed specifically for survivors with spinal cord injury

BEHAVIORAL

Watch landscape videos

A set of landscape videos

Sponsors & Collaborators

  • The Hong Kong Polytechnic University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-03-01
Primary Completion
2026-06-30
Completion
2026-06-30

Countries

  • Hong Kong

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06708026 on ClinicalTrials.gov