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Completed

NCT Number: NCT06673147

Effects of Nordic Walking on Prenatal Health

This randomized controlled trial (RCT) aimed to evaluate the effects of Nordic walking (NW) on gait kinematics, musculoskeletal pain, and quality of life in pregnant women.

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Key information

Age range

20 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Department of Health and Rehabilitation Sciences, Prince Sattam bin Abdulaziz University.

Riyadh, Alkharj, 11942, Saudi Arabia

About this study

Healthy pregnant women (N=50), aged 20-40 years and between 13 and 28 weeks of gestation, experiencing mild to moderate musculoskeletal pain, will be recruited. Participants will be randomized into either an intervention group (NW training) or a control group receiving standard prenatal care. The intervention group will undergo a 4-week learning phase followed by an 8-week NW program (3 sessions per week, 45 minutes per session), led by a certified instructor. Outcome measures will be assessed at baseline, after 4 weeks, and post-intervention (8 weeks), including spatiotemporal gait parameters (will be assessed using the GAITRite system), musculoskeletal pain (will be measured via Visual Analog Scale, VAS), and quality of life (will be measured using the SF-36 Health Survey).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy women aged 20 to 40 between 13 and 28 weeks into singleton pregnancy.
  • Participants must be experiencing mild to moderate musculoskeletal discomfort, such as lower back or pelvic pain,
  • Participants have no prior musculoskeletal or neurological diseases.
  • They must have no contraindications to exercising throughout pregnancy, as established by obstetrician clearance, and be able to engage in moderate physical activity under medical recommendations

Exclusion criteria

  • History of diseases affecting bony structures or lumbar intervertebral discs.
  • Pain caused by non-musculoskeletal factors (such as urinary tract infections or obstetric complications).
  • Multiple pregnancies, pre-existing mobility conditions, and high-risk pregnancies or complications that restrict physical activity.

Treatment and study plan

Prenatal Nordic Walking

Other

Traditional Nordic walking poles will be modified according to International Nordic Walking Federation guidelines, which meant that the elbows were bent at a 90°angle when holding the poles in a vertical position. Nordic Walking will be conducted in two phases consisting of a 4-week learning phase followed by an 8-week main phase of intervention.

Primary outcomes

  1. Spatial gait parameters

    Time frame: 20 minutes

    A GAITRite system will be used to assess the spatial parameters of gait

  2. Temporal parameters of gait

    Time frame: 20 minutes

    A GAITRite system will be used to assess the temporal parameters of gait

Secondary outcomes

  1. Visual Analog Score for musculoskeletal pain

    Time frame: 5 minutes

    The Visual Analog Score is depicted as a 10 cm horizontal line divided into 1 cm sections, each representing 1 point, resulting in a score ranging from 0 to 10 points. Higher scores mean worse outcome.

  2. Quality of life

    Time frame: 10 minutes

    The SF-36 Health Survey will be used to determine the results.

Sponsors and collaborators

Lead sponsor

University of Jazan

Other Gov

Registry information

Official study title

Effects of Nordic Walking on Prenatal Health: A Focus on Gait Kinematics, Musculoskeletal Pain, and Quality of Life. A Randomized Controlled Trial.

Acronym: Nordic Walking

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 4, 2024
Registry last updated
Jul 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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