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PhysiotherapistNCT06993909

Clinical Approaches to Stretching Intensity in Post-Operative Knee Rehabilitation

An observational study of Physiotherapist, run by Acibadem University at 1 site in Turkey (Türkiye).

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study aims to examine how physiotherapists determine stretching intensity during knee flexion exercises in post-operative rehabilitation. It will also explore professional and clinical factors influencing these decisions, with the goal of informing standardized rehabilitation protocols. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Physiotherapist
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
26 May 2025to 15 Jul 2025
Phase
Observational
Are there results?
Not yet: the study is under way

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: Licensed physiotherapists in Türkiye with at least one year of clinical experience who have worked with post-operative knee rehabilitation patients within the past year.

Who may be able to join

  • Physiotherapists with at least 1 year of clinical experience
  • Involved in post-operative knee rehabilitation in the past year
  • Willing to participate voluntarily

Who cannot join

  • Refusal to participate
  • Incomplete or inconsistent questionnaire responses

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Ali Ömer Acar, PT, MSc, PhD(c) contact

0216 500 44 44 ext. 3578

aliomeracar@gmail.com

Turkey (Türkiye)1 site
  • Acıbadem University

    Ataşehir, Istanbul, 34752

    Ali Ömer Acar, Pt. Msc. PhD(c), 0216 500 44 44 ext. 3578, aliomeracar@gmail.com

Other trials in Turkey (Türkiye)

About this study

This study aims to examine how physiotherapists determine stretching intensity during knee flexion exercises in post-operative rehabilitation. It will also explore professional and clinical factors influencing these decisions, with the goal of informing standardized rehabilitation protocols.

Read the detailed description

This study aims to comprehensively evaluate the approaches of physiotherapists actively involved in post-operative knee rehabilitation in determining stretching intensity during knee flexion exercises. It also seeks to identify the professional and clinical factors influencing these decisions. By revealing the variations between physiotherapists' perceptions and their actual clinical practices regarding stretching intensity, the study aims to contribute to the development of standardized clinical protocols and enhance the specificity of existing rehabilitation guidelines.

Conditions
Physiotherapist
Keywords
Stretching, Post-Operative, Rehabilitation, Clinical Decision-Making

What participants receive

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

Study groups in NCT06993909
Study groupRoleWhat they receive
PhysiotherapistsLicensed physiotherapists with at least one year of clinical experience who have worked in post-operative knee rehabilitation within the past year. Participants will complete a one-time online or in-person questionnaire regarding their clinical decision-making on stretching intensity.

What is being measured

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

  1. Stretching Intensity in Post-Operative Knee Rehabilitation

    Primary outcome includes the duration, frequency, and maximum allowable pain/discomfort levels (measured using Visual Analog Scale) of passive knee flexion stretching exercises used by physiotherapists in post-operative rehabilitation. Data will be collected through a structured questionnaire.

    Measured: At time of questionnaire completion (single time point)

Timeline

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

  1. First posted29 May 2025
  2. Study start26 May 2025 (estimated)
  3. Primary completion1 Jul 2025 (estimated)
  4. Study completion15 Jul 2025 (estimated)

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
Other
Time perspective
Cross-sectional
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06993909
Sponsor's protocol ID
ACU-FTR-AOA2
Status last verified
May 2025
First submitted
20 May 2025
Last updated
29 May 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Anonymized individual participant data (IPD) collected through the questionnaire will be made available for academic and research purposes upon reasonable request. No personally identifiable information will be included in the shared dataset.

Questions about this trial

What is this clinical trial studying?

An observational study of Physiotherapist, run by Acibadem University at 1 site in Turkey (Türkiye).

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 3 inclusion and 2 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: opening soon, as of the sponsor's last update on 29 May 2025. 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 Turkey (Türkiye). 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Ali Ömer Acar, PT, MSc, PhD(c) (0216 500 44 44 ext. 3578, aliomeracar@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Stretching Intensity in Post-Operative Knee Rehabilitation (time frame: At time of questionnaire completion (single time point)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 29 May 2025.

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