NCT07840755

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
0mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress67%
Sep 2026Oct 2026

Study Start

First participant enrolled

September 6, 2026

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

September 20, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 25, 2026

Completed
23 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 18, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 18, 2026

Last Updated

September 25, 2026

Status Verified

September 1, 2026

Enrollment Period

1 month

First QC Date

September 20, 2026

Last Update Submit

September 20, 2026

Conditions

Keywords

Nordic Pole WalkingForward Head PostureNeck PainPulmonary FunctionRespiratory Muscle StrengthCraniovertebral Angle

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

EXPERIMENTAL

Participants assigned to this group will perform Nordic pole walking for 6 weeks, 3 sessions per week, with each session lasting 40 minutes.

Behavioral: Nordic Pole Walking

General Walking Group

ACTIVE COMPARATOR

Participants assigned to this group will perform general walking for 6 weeks, 3 sessions per week, with each session lasting 40 minutes.

Behavioral: General Walking

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.

Also known as: Nordic Walking
Nordic Pole Walking Group
General WalkingBEHAVIORAL

Participants will perform general walking for 6 weeks, 3 sessions per week, with each session lasting 40 minutes.

General Walking Group

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Neck Pain

Interventions

Nordic Walking

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

WalkingLocomotionMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological PhenomenaExerciseMotor Activity

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to either a Nordic pole walking group or a general walking group.
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

Locations