Effect of Home-based Exercise Program on Visual Reliance, Cervical Spine Proprioception, and Postural Stability in Older Adults With Forward Head Posture
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Loma Linda University
- Enrollment
- 21
- Locations
- 1
- Primary Endpoint
- Change in Cervical Joint Position Error (JPE)
Study Overview
Brief 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.
Detailed Description
This study will have a sample size of 50 older adults (males and females) aged 65-74 years old with FHP. This sample size will provide us with enough power to detect the needed effect size (medium effect size). The estimated attrition rate is 20%. The participants will be recruited from the local community through flyers, e-mails, and word of mouth. Study flyers will be delivered to physical therapy clinics, physician offices, and support groups with verbal description for further explanations. Potential participants who respond to the emails or flyers will be provided with a verbal description of the study.
The study will be conducted in the Department of Physical Therapy, Loma Linda University, Loma Linda. Hard copies will be stored in a locked file cabinet in a locked research laboratory and computer data will be stored on an encrypted computer in a locked research laboratory.
All data will be analyzed using Statistical Package for the Social Sciences (SPSS) version 27.0. For quantitative data, the investigators will use the General Linear Model (Mixed Factorial Analysis of Variance) and Correlation Analysis (Pearson's Correlation). Also, a statistician will be consulted to accurately analyze and interpret results. The alpha level will be set at 0.05.
Efforts will be made to keep participants' personal information confidential, but the investigators cannot guarantee absolute confidentiality. The investigators will use a pseudonym throughout the study for all recorded data so participant's actual name will not be used. Participants will not be identified by name in any publications describing the results of this study. Data in hard copy will be kept in a locked file cabinet in a locked office and electronic data will be password protected.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 65 Years to 74 Years (Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
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
- •Cervical spine surgery
- •Any falls in past six months
- •Medications causing frequent dizziness
- •Any health care for neck, shoulder, or low back pain past 12 months
- •Greater than minimal neck pain as determined by the Visual Analogue Scale (VAS) > 3/10
- •Neck Disability Index (NDI) > 15%
- •Forward Head Angle (FHA) < 46 degrees
- •Forward Shoulder Angle (FSA) < 52 degrees
Arms & Interventions
Single group
The study will include one group and each participant will perform home-based exercise for 8-weeks.
Intervention: Home-based Exercise Program (Other)
Outcomes
Primary Outcomes
Change in Cervical Joint Position Error (JPE)
Time Frame: JPE will be measured twice (pre vs post-intervention) and each time will take approximately 25-30 minutes.
Ability to relocate one's head and neck to pre-determined neutral position recorded in degrees.
Change in Active Cervical Spine Range of Motion (AROM)
Time Frame: AROM will be measured twice (pre vs post-intervention) and each time will take approximately 5 minutes
Ability to actively move cervical spine in all six directions (flexion, extension, right and left rotation, right and left Lateral flexion). Cervical AROM will be measured in degrees.
Change in Postural Stability
Time Frame: Postural stability will be measured twice (pre vs post-intervention) and each time will take approximately 25 minutes
Ability to keep center of gravity within base of support under six different testing conditions and will be scored from 0-100 by the computer software. Higher scores indicate better postural stability.
Change in Forward Head Angle (FHA)
Time Frame: FHA will be measured twice (pre vs post-intervention) and each time will take approximately 13 minutes.
FHA is the angle formed between a line extending from the tragus to C7 and a vertical axis at C7. FHA will be measured in degrees.
Change in Forward Shoulder Angle (FSA)
Time Frame: FSA will be measured twice (pre vs post-intervention) and each time will take approximately 13 minutes.
FSA is the angle between a line extending from C7 to acromion and the vertical axis at C7. FSA will be measured in degrees.
Post-Intervention Structured Interview
Time Frame: 20-25 minutes
Post-intervention structured interview will be conducted using open-ended questions. Interviews will be recorded and transcribed verbatim. Transcriptions will be individually coded, and then group coded using qualitative research software.
Secondary Outcomes
- Change in Balance Confidence(ABC-6 will be conducted twice (pre vs post-intervention) and each time will take approximately 5 minutes.)