CompletedNot Applicable

Effect of Postural Realignment on Postural Stability and Visual Reliance in Older Adults

United States21 participantsStarted 2022-01-12

Plain-language summary

The purpose of this investigator-initiated study is 1) to investigate correlation between cervical spine joint position error (JPE) and postural stability in asymptomatic older adults with forward head posture (FHP), 2) to examine the effect of a home-based exercise program on visual reliance and cervical spine proprioception for postural stability in asymptomatic older adults with FHP, 3) to study the effect of immediate postural correction on cervical spine JPE and active range of motion (AROM), and 4) to determine participant post-intervention perception of changes in FHP, postural stability and effect on quality of life.

Who can participate

Age range

65 Years – 74 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Older adults aged 65-74 years with forward head posture (FHP)
. Live independently
. No use of assistive devices for ambulation
. Have interest in correcting misaligned posture
. Normal Physical Activity Readiness Questionnaire (PAR-Q+)

Exclusion criteria

. Neurologic deficits
. Disorders causing dizziness

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Change in Cervical Joint Position Error (JPE)

Timeframe: JPE will be measured twice (pre vs post-intervention) and each time will take approximately 25-30 minutes.

Change in Active Cervical Spine Range of Motion (AROM)

Timeframe: AROM will be measured twice (pre vs post-intervention) and each time will take approximately 5 minutes

Change in Postural Stability

Timeframe: Postural stability will be measured twice (pre vs post-intervention) and each time will take approximately 25 minutes

Change in Forward Head Angle (FHA)

Timeframe: FHA will be measured twice (pre vs post-intervention) and each time will take approximately 13 minutes.

Change in Forward Shoulder Angle (FSA)

Timeframe: FSA will be measured twice (pre vs post-intervention) and each time will take approximately 13 minutes.

Post-Intervention Structured Interview

Timeframe: 20-25 minutes

Trial details

NCT IDNCT05032274

SponsorLoma Linda University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-03-03

View on ClinicalTrials.gov More Forward Head Posture trials