Effects of Nordic Pole Walking in Adults With Forward Head Posture
1 other identifier
interventional
44
1 country
1
Brief Summary
This randomized controlled trial aims to investigate the effects of Nordic pole walking on pain, neck-related disability, pulmonary function, respiratory muscle strength, and postural alignment in adults with forward head posture and neck pain. Participants will be randomly assigned to either a Nordic pole walking group or a general walking group. Both groups will participate in a 6-week walking program, three times per week, with each session lasting 40 minutes. Neck-related disability and pain will be assessed using the Neck Disability Index (NDI) and Visual Analog Scale (VAS). Pulmonary function will be assessed using forced vital capacity (FVC), forced expiratory volume in one second (FEV1), and the FEV1/FVC ratio. Respiratory muscle strength will be evaluated using maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP), and postural alignment will be assessed using the craniovertebral angle (CVA). Measurements will be performed before and after the 6-week intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2026
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
September 6, 2026
CompletedFirst Submitted
Initial submission to the registry
September 20, 2026
CompletedFirst Posted
Study publicly available on registry
September 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 18, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 18, 2026
September 25, 2026
September 1, 2026
1 month
September 20, 2026
September 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Visual Analog Scale (VAS) for Neck Pain
Neck pain intensity will be assessed using a 10-cm horizontal Visual Analog Scale (VAS). The left end of the line represents no pain (0), and the right end represents very severe pain (10). To minimize bias, numerical values will not be displayed on the line. Participants will mark the point that best represents their perceived pain intensity, and the distance from the left end to the marked point will be measured with a ruler. Higher scores indicate greater pain intensity.
Baseline and 6 weeks
Neck Disability Index (NDI)
Neck-related disability will be assessed using the Neck Disability Index (NDI), a 10-item self-reported questionnaire. Each item is scored from 0 to 5, resulting in a raw total score ranging from 0 to 50. The raw total score will be multiplied by 2 and converted to a 0-100 scale, with higher scores indicating greater neck-related disability. The change in NDI score from baseline to 6 weeks will be evaluated.
Baseline and 6 weeks
Secondary Outcomes (6)
Forced Vital Capacity (FVC)
Baseline and 6 weeks
Forced Expiratory Volume in One Second (FEV1)
Baseline and 6 weeks
FEV1/FVC Ratio
Baseline and 6 weeks
Maximal Inspiratory Pressure (MIP)
Baseline and 6 weeks
Maximal Expiratory Pressure (MEP)
Baseline and 6 weeks
- +1 more secondary outcomes
Study Arms (2)
Nordic Pole Walking Group
EXPERIMENTALParticipants assigned to this group will perform Nordic pole walking for 6 weeks, 3 sessions per week, with each session lasting 40 minutes.
General Walking Group
ACTIVE COMPARATORParticipants assigned to this group will perform general walking for 6 weeks, 3 sessions per week, with each session lasting 40 minutes.
Interventions
Participants will perform Nordic pole walking using Nordic walking poles for 6 weeks, 3 sessions per week, with each session lasting 40 minutes. Participants will walk with coordinated upper- and lower-extremity movements while actively planting and pushing the poles during walking.
Participants will perform general walking for 6 weeks, 3 sessions per week, with each session lasting 40 minutes.
Eligibility Criteria
You may qualify if:
- Adults aged 20 years or older
- Craniovertebral angle (CVA) \< 50°
- Neck pain lasting at least 3 months
- Visual Analog Scale (VAS) score \> 4
You may not qualify if:
- Individuals currently participating in an exercise program related to neck pain management or postural correction
- Individuals with musculoskeletal disorders that limit the ability to perform the exercise intervention
- Individuals with respiratory diseases such as asthma, chronic obstructive pulmonary disease (COPD), bronchiectasis, or pneumonia
- Individuals who have been regular smokers within the past 6 months
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sahmyook University
Seoul, 01795, South Korea
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
September 20, 2026
First Posted
September 25, 2026
Study Start
September 6, 2026
Primary Completion (Estimated)
October 18, 2026
Study Completion (Estimated)
October 18, 2026
Last Updated
September 25, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share