Passive Static Stretching for Improving Hip Range of Motion in Patients and Healthy Individuals
HIP- STR
Effects Of Passive Static Stretching On Hip Range Of Motion In Patients With Joint Pathologies And Healthy Individuals: A Pilot Study
1 other identifier
observational
12
1 country
1
Brief 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. 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Nov 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 3, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 3, 2025
CompletedFirst Submitted
Initial submission to the registry
March 22, 2026
CompletedFirst Posted
Study publicly available on registry
March 27, 2026
CompletedMarch 27, 2026
March 1, 2026
25 days
March 22, 2026
March 22, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (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.
4 weeks (pre- and post-intervention)
Study Arms (3)
Hip Arthroplasty Patients
Patients 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 Patients
Patients 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 Subjects
Healthy individuals without hip pathologies. Intervention: passive static stretching applied to hip joint. Flexibility measured before and after stretching sessions.
Eligibility Criteria
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.
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Osteopathy and Clinical Kinesiology Practice
Roma, RM, 00195, Italy
Related Publications (5)
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.
PMID: 32393301BACKGROUNDHopewell 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.
PMID: 40228833BACKGROUNDYildirim 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.
PMID: 26929476BACKGROUNDLempke 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.
PMID: 28182516BACKGROUNDBehm 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.
PMID: 21373870BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
Emanuele Novelli, MSc Kinesiology, Osteopath
OmicronBeta Research
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Doctor of Clinical Kinesiology and Osteopathy
Study Record Dates
First Submitted
March 22, 2026
First Posted
March 27, 2026
Study Start
November 3, 2025
Primary Completion
November 28, 2025
Study Completion
December 3, 2025
Last Updated
March 27, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
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.