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Clinical Trials in Canada / NCT07288684
Recruiting Not applicable

Chiropractor Delivered Virtual Intervention After Vertebral frActure

NCT07288684 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-10-20
Last updated
2025-12-17

Condition(s) studied

OsteoporosisVertebral Fracture

Investigational drug(s) / intervention(s)

VIVA

VIVA: VIVA is an intervention for people with vertebral fractures that covers four areas: pain management, safe movement, exercise, and nutrition. It includes print and video resources, and a framework for goal setting, selecting exercises, and teaching body mechanics.

Study summary

This study will determine feasibility of a chiropractor delivered virtual intervention for individuals following osteoporotic vertebral fracture.

This pilot trial will have two parallel groups with a 1:1 ratio. Participants will be randomized to: 1) immediate receipt; or 2) waitlist usual care control and delayed receipt of VIVA 10 weeks post-randomization.

VIVA is an intervention for people with vertebral fractures that covers four areas: pain management, safe movement, exercise, and nutrition. It includes print and video resources, and a framework for goal setting, selecting exercises, and teaching body mechanics.

A chiropractor (DC) completes a virtual assessment and then leads twelve 1:1 virtual sessions (via Zoom) over eight weeks. Sessions start with brief education on a topic (e.g., safe movement, pain management, exercise, nutrition), followed by training and modeling of exercise and safe movement strategies, then goal setting, and action planning.

This trial will be considered feasible if a) we recruit 14 people in eight months; b) 80% of participants complete the trial; and c) exercise adherence is 75%.

Eligibility

Sex
ALL
Min age
50 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Over the age of 50 (men or post-menopausal women) * Have had a vertebral fracture in the past two years * Willing to participate in twelve (12) virtual rehabilitation sessions for 10 weeks * Have access to internet and a smart device with a camera and microphone Exclusion Criteria: * Cauda equina syndrome or spinal cord injury * Had a traumatic fracture (i.e., car accident) * An active infection * Active inflammatory arthritis with a flare up within the past two years * An inability to follow two-step commands or understand instructions and are without a caregiver to support participation * Been participating in a similar rehabilitation program for vertebral fractures delivered by a physical therapist, exercise physiologist or kinesiologist and includes exercise * Any surgeries planned or health problems that might cause their health to change significantly in the next 3 months

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Waterloo Waterloo Ontario Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07288684 on ClinicalTrials.gov ↗ ← All trials in Canada