NCT06673147

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
55

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

November 1, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

November 4, 2024

Completed
1 day until next milestone

Study Start

First participant enrolled

November 5, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 6, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 29, 2025

Completed
Last Updated

July 8, 2025

Status Verified

November 1, 2024

Enrollment Period

6 months

First QC Date

November 1, 2024

Last Update Submit

July 7, 2025

Conditions

Keywords

Prenatal health Nordic walkingpregnancymusculoskeletal paingait parametersquality of life

Outcome Measures

Primary Outcomes (2)

  • Spatial gait parameters

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

    20 minutes

  • Temporal parameters of gait

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

    20 minutes

Secondary Outcomes (2)

  • Visual Analog Score for musculoskeletal pain

    5 minutes

  • Quality of life

    10 minutes

Study Arms (2)

Intervention group

EXPERIMENTAL

It will be receiving Nordic walking training

Other: Prenatal Nordic Walking

Control Group

NO INTERVENTION

This group will receive a standard prenatal care, which included routine obstetric check-ups and general advice on physical activity

Interventions

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.

Intervention group

Eligibility Criteria

Age20 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

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

Riyadh, Alkharj, 11942, Saudi Arabia

Location

MeSH Terms

Conditions

Musculoskeletal Pain

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Nadia L Radwan, PHD

    Prince Sattam Bin Abdulaziz University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Out of 50 pregnant women who will be screened for their eligibility criteria, The participants will be randomized to either intervention group (Nordic Walking) or control group (standard prenatal care).
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

November 1, 2024

First Posted

November 4, 2024

Study Start

November 5, 2024

Primary Completion

May 6, 2025

Study Completion

June 29, 2025

Last Updated

July 8, 2025

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

Locations