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Completed

NCT Number: NCT07495371

Passive Static Stretching for Improving Hip Range of Motion in Patients and Healthy Individuals

This pilot study evaluates whether passive static stretching can improve hip movement in three groups: people who have had hip replacement surgery, individuals with long-term hip pain, and healthy volunteers. Participants will follow a 4-week stretching program, doing exercises three times per week under the supervision of a trained clinician. Hip range of motion will be measured before and after the program using accurate electronic sensors. The goal is to determine if passive static stretching is a safe and effective way to increase hip flexibility and support daily activities. The study involves no new medications or invasive procedures and is considered low risk.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Osteopathy and Clinical Kinesiology Practice

Roma, RM, 00195, Italy

About this study

This pilot study investigates the effects of passive static stretching on hip range of motion (ROM) in three populations: patients who have undergone total hip arthroplasty (THA), individuals with chronic non-surgical hip pain, and healthy volunteers. A total of 12 participants will be enrolled, divided equally into three groups.

Participants will follow a four-week stretching program, performing assisted hip flexion and abduction exercises three times per week, with each stretch held for 30 seconds. All sessions are supervised by a trained kinesiologist to ensure proper alignment, submaximal intensity, and participant safety.

Hip ROM will be measured pre- and post-intervention using high-precision triaxial electronic sensors (accelerometers and gyroscopes) under standardized conditions. The study will track changes in hip flexion and abduction, monitor for adverse events, and assess compliance.

The purpose is to explore whether passive static stretching is a safe, feasible, and effective method to enhance hip mobility across different populations, providing preliminary data for future larger studies.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Adults able to participate in a 4-week passive hip stretching protocol
  • No contraindications to passive hip stretching
  • No neurological or musculoskeletal comorbidities affecting motor control
  • Willingness and ability to provide written informed consent

Exclusion criteria

  • Presence of neurological or musculoskeletal conditions that impair hip movement or motor control
  • Contraindications to stretching (e.g., recent surgery not related to hip arthroplasty, acute injuries)
  • Inability or unwillingness to complete the full 4-week study protocol

Treatment and study plan

Primary outcomes

  1. Hip Range of Motion (Flexion and Abduction)

    Time frame: 4 weeks (pre- and post-intervention)

    Hip ROM was measured using high-precision triaxial electronic sensors equipped with accelerometers and gyroscopes (Sensorize). Participants were assessed in standardized positions over the hip joint, with data sampled at 200 Hz to determine maximal flexion and abduction angles. Measurements were taken pre- and post-intervention across all groups.

Sponsors and collaborators

Lead sponsor

Omicron beta research

Other

Registry information

Official study title

Effects Of Passive Static Stretching On Hip Range Of Motion In Patients With Joint Pathologies And Healthy Individuals: A Pilot Study

Acronym: HIP- STR

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Mar 27, 2026
Registry last updated
Mar 27, 2026

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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