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Hip Joint DisordersHIP- STRNCT07495371

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

An observational study of Hip Joint Disorders and Recovery After Total Hip Arthroplasty, run by Omicron beta research at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
How many people
12 participants
Where
1 siteItaly
Study dates
3 Nov 2025to 3 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: The study included 12 adult participants (7 women, 5 men; mean age 52.5 ± 6.8 years) divided into three groups: Group A: 4 patients who had undergone total hip arthroplasty (THA) Group B: 4 patients with chronic non-surgical hip pain Group C: 4 healthy individuals with no prior hip or joint pathology Participants were selected based on their ability to safely perform passive hip stretching, absence of neurological or musculoskeletal comorbidities affecting motor control, and willingness to complete the 4-week intervention protocol. Written informed consent was obtained from all participants.

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Osteopathy and Clinical Kinesiology Practice

    Roma, RM, 00195

Other trials in Italy

About this study

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

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.

Read the detailed description

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.

Keywords
Hip stretching, ROM improvement, Hip arthroplasty, Healthy subjects, Pilot rehabilitation study, Flexibility assessment

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07495371
Study groupRoleWhat they receive
Hip Arthroplasty PatientsPatients who underwent hip arthroplasty. Intervention: passive static stretching to improve hip range of motion (ROM). Assessment of flexibility before and after stretching sessions.
Chronic Hip Pain PatientsPatients with chronic hip pain not due to arthroplasty. Intervention: passive static stretching to evaluate improvement in hip ROM. Pre- and post-intervention flexibility assessments performed.
Healthy SubjectsHealthy individuals without hip pathologies. Intervention: passive static stretching applied to hip joint. Flexibility measured before and after stretching sessions.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hip Range of Motion (Flexion and Abduction)

    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.

    Measured: 4 weeks (pre- and post-intervention)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Mar 2026
  2. Study start3 Nov 2025
  3. Primary completion28 Nov 2025
  4. Study completion3 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
12 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07495371
Sponsor's protocol ID
HIP-STRETCH- 2025- 01
Acronym
HIP- STR
Status last verified
Mar 2026
First submitted
22 Mar 2026
Last updated
27 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared to protect participant privacy and confidentiality. Given the small sample size and sensitive nature of the measurements, sharing raw data could potentially allow identification of participants. Data will be used solely for the purposes of this study.

Publications

  • Kobsar D, Charlton JM, Tse CTF, Esculier JF, Graffos A, Krowchuk NM, Thatcher D, Hunt MA. Validity and reliability of wearable inertial sensors in healthy adult walking: a systematic review and meta-analysis. J Neuroeng Rehabil. 2020 May 11;17(1):62. doi: 10.1186/s12984-020-00685-3.

    PubMed 32393301
  • Hopewell S, Chan AW, Collins GS, Hrobjartsson A, Moher D, Schulz KF, Tunn R, Aggarwal R, Berkwits M, Berlin JA, Bhandari N, Butcher NJ, Campbell MK, Chidebe RCW, Elbourne D, Farmer A, Fergusson DA, Golub RM, Goodman SN, Hoffmann TC, Ioannidis JPA, Kahan BC, Knowles RL, Lamb SE, Lewis S, Loder E, Offringa M, Ravaud P, Richards DP, Rockhold FW, Schriger DL, Siegfried NL, Staniszewska S, Taylor RS, Thabane L, Torgerson D, Vohra S, White IR, Boutron I. CONSORT 2025 statement: updated guideline for reporting randomised trials. BMJ. 2025 Apr 14;389:e081123. doi: 10.1136/bmj-2024-081123.

    PubMed 40228833
  • Yildirim MS, Ozyurek S, Tosun O, Uzer S, Gelecek N. Comparison of effects of static, proprioceptive neuromuscular facilitation and Mulligan stretching on hip flexion range of motion: a randomized controlled trial. Biol Sport. 2016 Mar;33(1):89-94. doi: 10.5604/20831862.1194126. Epub 2016 Feb 8.

    PubMed 26929476
  • Lempke L, Wilkinson R, Murray C, Stanek J. The Effectiveness of PNF Versus Static Stretching on Increasing Hip-Flexion Range of Motion. J Sport Rehabil. 2018 May 1;27(3):289-294. doi: 10.1123/jsr.2016-0098. Epub 2018 May 22.

    PubMed 28182516
  • Behm DG, Chaouachi A. A review of the acute effects of static and dynamic stretching on performance. Eur J Appl Physiol. 2011 Nov;111(11):2633-51. doi: 10.1007/s00421-011-1879-2. Epub 2011 Mar 4.

    PubMed 21373870

Questions about this trial

What is this clinical trial studying?

An observational study of Hip Joint Disorders and Recovery After Total Hip Arthroplasty, run by Omicron beta research at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Hip Range of Motion (Flexion and Abduction) (time frame: 4 weeks (pre- and post-intervention)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07495371, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Mar 2026.

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