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Home-Based Exercise for Forward Head Posture
N/A
Recruiting
Led By Eric G Johnson, DSc
Research Sponsored by Loma Linda University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
No use of assistive devices for ambulation
Be older than 65 years old
Must not have
Greater than minimal neck pain as determined by the Visual Analogue Scale (VAS) > 3/10
Medications causing frequent dizziness
Timeline
Screening 3 weeks
Treatment Varies
Follow Up jpe will be measured twice (pre vs post-intervention) and each time will take approximately 25-30 minutes.
Awards & highlights
Summary
This trial will investigate whether there is a correlation between neck pain and posture in older adults, as well as whether an exercise program can help improve posture and neck pain.
Who is the study for?
This trial is for older adults aged 65-74 with forward head posture who live independently, do not use walking aids, and are interested in improving their posture. They must be physically ready for exercise as per the PAR-Q+ and have no recent falls, neck pain or surgeries, dizziness disorders, or related healthcare within the last year.Check my eligibility
What is being tested?
The study tests a home-based exercise program's effect on balance and reliance on vision in older adults with forward head posture. It aims to see if exercises can improve neck joint awareness and overall stability without visual cues.See study design
What are the potential side effects?
Since this trial involves a non-invasive home exercise program designed for older adults, side effects may include muscle soreness or fatigue due to new physical activities but should generally be minimal.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can walk without any help from devices.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My neck pain is more than minimal, scoring over 3 on a pain scale.
Select...
My medication often makes me feel dizzy.
Select...
I have problems with my nervous system.
Select...
I have had surgery on my neck spine.
Select...
I experience dizziness due to a health condition.
Select...
My shoulder angle is less than 52 degrees.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ jpe will be measured twice (pre vs post-intervention) and each time will take approximately 25-30 minutes.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~jpe will be measured twice (pre vs post-intervention) and each time will take approximately 25-30 minutes.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Active Cervical Spine Range of Motion (AROM)
Change in Cervical Joint Position Error (JPE)
Change in Forward Head Angle (FHA)
+3 moreSecondary outcome measures
Change in Balance Confidence
Trial Design
1Treatment groups
Experimental Treatment
Group I: Single groupExperimental Treatment1 Intervention
The study will include one group and each participant will perform home-based exercise for 8-weeks.
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Who is running the clinical trial?
Loma Linda UniversityLead Sponsor
308 Previous Clinical Trials
261,070 Total Patients Enrolled
Eric G Johnson, DScPrincipal InvestigatorLoma Linda University
1 Previous Clinical Trials
21 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- My neck pain is more than minimal, scoring over 3 on a pain scale.My medication often makes me feel dizzy.I have problems with my nervous system.I want to correct my posture.I can walk without any help from devices.I am between 65 and 74 years old and have a forward-leaning head posture.I have sought treatment for neck, shoulder, or low back pain in the last year.I have had surgery on my neck spine.I live on my own without needing daily help.I experience dizziness due to a health condition.My shoulder angle is less than 52 degrees.
Research Study Groups:
This trial has the following groups:- Group 1: Single group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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