NCT06296771

The Effect of a Combined Aerobic and Resistance Exercise (CARE) Training Programme on Cardiometabolic Outcomes in Individuals With Chronic Spinal Cord Injury: A Randomised Controlled Trial

University of Bath·ClinicalTrials.gov·otherNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Spinal Cord Injury
Drug/Device/Intervention
Dietary energy restriction group (D)
Study type
Interventional
Intervention type
other
Sponsor & location
Primary sponsor
University of Bath
Location
Bath, United Kingdom
Timeline & enrollment
Phase
N/A
Start date
May 22, 2024
End date
May 22, 2025
Enrollment
21 participants
Primary outcome

Lipid profile,Fasting insulin concentration,Insulin sensitivity

Summary

The goal of this study is to investigate the effectiveness of an 8-week dietary energy
 restriction with exercise or dietary energy restriction alone on the cardiometabolic health
 outcomes of individuals with chronic spinal cord injury. This study is a randomised
 controlled trial conducted at a single centre, consisting of two parallel arms. The main
 questions it aims to answer are:
 
 1. the effectiveness of an 8-week dietary energy restriction with exercise or dietary
 energy restriction alone on cardiometabolic disease biomarker outcomes in individuals
 with chronic SCI
 
 2. the effectiveness of an 8-week dietary energy restriction with exercise or dietary
 energy restriction alone on fitness and health outcomes.
 
 Twenty-one participants will be randomly assigned in a 2:1 allocation ratio. The participants
 will be assigned to either the dietary energy restriction and exercise group (D+E) group,
 which combines dietary energy restriction and exercise intervention, or the dietary energy
 restriction group (D) group, which just undergoes dietary energy restriction using sealed
 envelopes.

ICD-10 classifications
Sequelae of injury of spinal cordOther injury of lumbar spinal cordInjury of spinal cord, level unspecifiedOther and unspecified injuries of thoracic spinal cordOther and unspecified injuries of cervical spinal cord
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06296771
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06296771 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Bath and is currently Not yet recruiting. The study focuses on Spinal Cord Injury. Target enrollment is 21 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.