CClinicalTrials.gg
TerminatedNCT05027178Updated Feb 17, 2023

Stroke Patients Receiving Chiropractic Care Post-rehabilitation

An interventional study of Chiropractic Care in Stroke, sponsored by Life University. Terminated at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-02-17.

Sponsored by Life University · Not applicable, Interventional, and Supportive care

Why this study was terminated
The study is being reformatted and will have a different protocol for the relaunch.

From the registry’s dates

  • Registered 1 year after the study started (first participant enrolled Aug 2020, registered Aug 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
6
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

The Life University Center for Chiropractic Research is conducting a research study to better understand how 12-weeks of chiropractic care differentially affects the post-rehabilitation brain electrical patterns and body movement patterns of individuals who have experienced hemorrhagic versus ischemic stroke The study will involve visits to the Life University Center for Chiropractic Research (CCR) in midtown Atlanta. During the 12 weeks of focused care, chiropractic visits could be several times a week depending on the care plan. In addition to the chiropractic care, individuals will receive a physical examination and three follow-up assessments. The assessments in the CCR will include a non-invasive evaluation of the brain wave patterns using electroencephalography (EEG), completion of a few surveys, a balance assessment and a movement assessment. Qualified individuals will receive study treatment and care at no cost.

02

Conditions studied

  • Stroke

Browse trials for

03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's enrollment of 6 is below the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Life University is the lead sponsor of 29 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Post stroke rehabilitation

Exclusion criteria

Exclusion Criteria:

  • Not experienced sub-arachnoid bleeding within the last 4 weeks, fractures or trauma to the skull, pregnancy, or progressive RA.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Single group
Masking
Single (Outcomes assessor)
Enrollment
6 participants (actual)

Study arms

  • Experimental
    Chiropractic care for Ischemic Stroke Patients

    12 weeks of full spine chiropractic care will be provided to patient. Patients may be asked to present one- two times per week.

    Other: Chiropractic Care

  • Experimental
    Chiropractic care for Hemorrhagic Stroke Patients

    12 weeks of full spine chiropractic care will be provided to patient. Patients may be asked to present one- two times per week.

    Other: Chiropractic Care

Interventions

  • OtherChiropractic Care

    Chiropractic care on stroke participants

06

What researchers measure

Primary outcomes

  1. Stroke Impact Scale Survey

    Disease specific self-report questionnaire that evaluates disability and health related quality of life post stroke.

    Time frame: Baseline

  2. Stroke Impact Scale Survey

    Disease specific self-report questionnaire that evaluates disability and health related quality of life post stroke.

    Time frame: 4 weeks

  3. Stroke Impact Scale Survey

    Disease specific self-report questionnaire that evaluates disability and health related quality of life post stroke.

    Time frame: 8 weeks

  4. Stroke Impact Scale Survey

    Disease specific self-report questionnaire that evaluates disability and health related quality of life post stroke.

    Time frame: 12 weeks

  5. Resting State Electroencephalography

    EEG assessment

    Time frame: Baseline

  6. Resting State Electroencephalography

    EEG assessment

    Time frame: 4 weeks

  7. Resting State Electroencephalography

    EEG assessment

    Time frame: 8 weeks

  8. Resting State Electroencephalography

    EEG assessment

    Time frame: 12 weeks

  9. Kinematic Assessment of Performance on finger to nose test

    Assessment to measure of dysmetria

    Time frame: Baseline

  10. Kinematic Assessment of Performance on finger to nose test

    Assessment to measure of dysmetria

    Time frame: 4 weeks

  11. Kinematic Assessment of Performance on finger to nose test

    Assessment to measure of dysmetria

    Time frame: 8 weeks

  12. Kinematic Assessment of Performance on finger to nose test

    Assessment to measure of dysmetria

    Time frame: 12 weeks

07

Study locations

1 site
  • Life University Center for Chiropractic Research
    Atlanta, Georgia 30308, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05027178
Lead sponsor
Life University
Responsible party
Sponsor
First posted
Aug 30, 2021
Start date
Aug 7, 2020
Primary completion
Nov 1, 2022
Completion
Nov 1, 2022
Last update
Feb 17, 2023

Study contacts

Stephanie Sullivan, DC, PhD
principal investigator · Life Univeristy

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion