Effects of Postural Education or Corrective Exercise on Forward Head Posture
The Effects of Postural Education or Corrective Exercise Intervention on the Craniovertebral Angle in Young Adults With Forward Head Posture: A Randomized Controlled Trial
2 other identifiers
interventional
79
1 country
1
Brief Summary
This randomized control trial examined the effects of postural education or corrective exercise intervention on the craniovertebral angle (CVA) in young adults with forward head posture (FHP). The objectives were 1: to investigate whether or not a corrective exercise program (CEP) consisting of self-myofascial release (SMR) + stretching; a CEP consisting of SMR + stretching + strengthening; or postural education (PE) had an effect on the CVA; 2. to determine which intervention yielded the greatest postural enhancement if a positive effect was observed in more than one intervention. \*\[note: SMR is a technique involving the self-application of pressure to fascia and muscle tissue for the purpose of enhancing flexibility, reducing muscle soreness, and influencing muscle relaxation\]. It was hypothesized that 4 weeks after receiving either CEP intervention or PE there would be a significant change in the CVA compared to a control group; and that there would be an intervention more effective than the others for improving the CVA. The null hypotheses were: there would be no CVA change after intervention in any of the groups; and there will be no intervention more effective than another for improving the CVA.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 26, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 4, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
November 4, 2021
CompletedFirst Submitted
Initial submission to the registry
March 18, 2022
CompletedFirst Posted
Study publicly available on registry
April 11, 2022
CompletedApril 11, 2022
April 1, 2022
2 months
March 18, 2022
April 4, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Craniovertebral Angle after 4 weeks
The angle between the intersection of two lines drawn on the photograph: the first line drawn from the tragus of the ear to the spinous process of C7 vertebrae and the second line drawn horizontally through C7 spinous process. In this study, a second researcher directly observed the primary investigator performing each CVA assessment, as well as provided verbal agreement with the accuracy of angle measurement. For each participant, the CVA was derived by taking the mean of two CVA measurements that were assessed on the captured photographs.
Baseline: On day 1 of study enrollment; Post-Intervention: Within 5 days after the end of the 4 week intervention period
Secondary Outcomes (2)
Midpoint Intervention Compliance
Assessed at the start of week 3
Endpoint Intervention Compliance
Within 5 days after the end of the 4 week intervention period.
Study Arms (4)
Posture Education (PE) Group
EXPERIMENTALPE group members received a 20-minute in-person one-on-one standardized educational session by a research team member in the laboratory on the following topics: health risks associated with forward head posture; postural guidelines for using mobile electronic devices, desktop computers, and laptop computers; as well as rest break guidelines. Participants were asked to adhere to the postural guidelines provided in the educational session for the next 4 weeks.
Self-Myofascial Release + Stretching (SMRS) Group
EXPERIMENTALThis group applied self-myofascial release (SMR) to their thoracic spine with a myofascial roller for 30 sec., then 6 repetitions of myofascial rolling for 90 sec. They applied SMR for 30 sec. to their neck flexors and extensors using their fingertips. They applied SMR to the upper trapezius and pectoralis for 30 sec using a soft tissue mobilization tool. For the first 2 weeks, they performed SMR 3x/wk. During wks. 3 and 4, they progressed SMR to 5 days/wk. Group members also performed stretching to these same muscles after SMR 3 days/wk for the first 2 weeks of the study, progressing to 5 days/wk during weeks 3 and 4.
Self-Myofascial Release + Stretching + Strengthening (SMRSS) Group
EXPERIMENTALThis group performed the same protocol as SMRS group, as well as include the following strengthening exercises: the supine chin tuck (SCT), upper thoracic-lower cervical extension (UTLCE) using an exercise band that provided 5.5 pounds of resistance, and a single-arm row with trunk rotation (SARTR) using exercise tubing that provided 20 pounds of resistance. The SCT was progressed in 3 phases: Week 1: chin tuck held 2 sec., 5 reps. Week 2: same as week 1, but included us of a towel roll placed under the head. Wks. 3 and 4: chin tuck with head lift 1 in., 2 sec. hold. UTLCE: neck extension with exercise band, held 2 sec. SARTR: single arm row with trunk rotation was performed in a controlled and fluid manner using a self-selected speed. The UTLCE and SARTR were performed with 1 X 10 reps for wks 1-2 and progressed to 2 X10 reps in wks 3-4. Strengthening exercises were performed 3x/wk. for 4 wks.
Control Group (CG)
NO INTERVENTIONParticipants in the CG did not receive an intervention.
Interventions
Please see arm description for a detailed description of the intervention
Please see arm description for a detailed description of the intervention
Eligibility Criteria
You may qualify if:
- Completion of informed consent
- Craniovertebral angle ≤ 53 degrees
- Self-rating of Transtheoretical Model stage of change stage ≥ 3/5
You may not qualify if:
- Any musculoskeletal injury to the head, shoulders, or spine within the last six months
- Diagnosis of pathology related to the cervical spine, thoracic spine, or upper extremities
- Non-clearance for physical activity based on results of the 2020 PAR-Q+ questionnaire
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Liberty Universitylead
- National Academy of Sports Medicinecollaborator
Study Sites (1)
Liberty University
Lynchburg, Virginia, 24515, United States
Related Publications (22)
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BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
David A Titcomb, DPT
Liberty University
- STUDY CHAIR
Bridget F Melton, EdD
Concordia University Chicago
- STUDY DIRECTOR
Theresa Miyashita, PhD
Concordia University Chicago
- STUDY DIRECTOR
Helen W Bland, PhD
Concordia University Chicago
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Health Sciences
Study Record Dates
First Submitted
March 18, 2022
First Posted
April 11, 2022
Study Start
August 26, 2021
Primary Completion
November 4, 2021
Study Completion
November 4, 2021
Last Updated
April 11, 2022
Record last verified: 2022-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
- Time Frame
- Starting immediately after publication. No end date.
- Access Criteria
- The primary investigator will review requests received by email. Requests granted to researchers and/or research institutions for the purpose of future research studies. The Liberty University Institutional Review Board will also be notified prior to releasing IPD and/or supporting information. Rather than a URL, individuals interested in IPD and/or supporting information will contact the primary investigator by email, which will be provided in the publication along with a statement about the plan to share IPD.
All collected IPD that underlie results in a publication.