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Muskuloskeletal DiseasesNCT07023809

Approaches to Chiropractic Care in Aging Patients

An observational study of Muskuloskeletal Diseases, run by Université du Québec à Trois-Rivières at 1 site in Canada.

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

The goal of this observational study is to understand how chiropractors adjust their therapeutic approaches based on their beliefs, the patient's age, and patient-specific characteristics, with a particular focus on aging patients. Read more about this study

Who is it for?
Any age
Conditions the study is for
Muskuloskeletal Diseases
How many people
12 participants
Where
1 siteCanada
Study dates
1 Aug 2025to 15 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
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Chiropractors practicing in private clinics in Québec who report treating adult and aging patients presenting with musculoskeletal disorders.

Who may be able to join

  • Be a practicing chiropractor working in a private clinic in Quebec located within approximately 150 km of the Université du Québec à Trois-Rivières.
  • Have a patient base mainly composed of younger adults (ages 18 to 49) and aging adults (50 years and older).
  • Use diversified manual therapy techniques on the spine and pelvis. This terminology is commonly used in chiropractic and refers to a range of techniques including spinal manipulation, spinal mobilization, instrument-assisted manipulation, and the use of pelvic blocks.
  • Be an adult aged between 18 and 49 years or 50 years and older.
  • Be a regular patient of the chiropractor.

Who cannot join

  • Not having a treatment room large enough to accommodate the researcher and her equipment, in addition to the patient.
  • Having a schedule that does not allow extending the duration of multiple treatments within a single day.
  • New patients, defined as those attending their first or second appointment at the clinic. These visits are typically longer, and it is reasonable to expect that the patient may have more questions during these initial sessions. The presence of a third party could be uncomfortable for a patient who is still adapting to a new type of care or a new chiropractor. We do not wish to interfere with a patient-chiropractor relationship that is still being established.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Department of Chiropractic, Université du Québec à Trois-Rivières

    Trois-Rivières, Quebec, G8Z4M3

Other trials in Canada

About this study

Official title: Exploration of Factors Influencing Chiropractors' Therapeutic Choices in the Management of Aging Patients: an Observational Study

The goal of this observational study is to understand how chiropractors adjust their therapeutic approaches based on their beliefs, the patient's age, and patient-specific characteristics, with a particular focus on aging patients. The study population includes licensed chiropractors in Quebec treating adult and aging patients in real clinical settings. Patients involved are receiving their usual care and are not the primary focus of the study.

The main questions it aims to answer are:

Read more
  • How do chiropractors modify their treatment strategies for aging patients?
  • What contextual and clinical factors influence these therapeutic decisions?

Researchers will observe chiropractors during routine care to assess treatment characteristics. To do this, participants will:

  • Use a sensor to measure the force applied during specific manual treatments.
  • Complete brief questionnaires after each treatment to report contextual details.
  • Allow for the presence of a researcher during treatment delivery for observational purposes.

Patients will:

  • Fill out a short pre-treatment questionnaire.
  • Receive their usual care with no interference in the treatment process.
  • Be informed in advance and free to decline participation at any point.

This study aims to provide a detailed picture of current chiropractic practices in Quebec related to the care of aging patients, while minimizing disruption to clinical routines.

Read the detailed description

Chiropractors play a key role in the management of musculoskeletal conditions in aging populations (Hawk et al., 2010). However, due to age-related physiological changes such as decreased bone density and increased tissue fragility, aging patients may face a higher risk of adverse effects from manual therapies-including fractures or hematomas. To ensure patient safety, clinical guidelines recommend adjusting both the selection and intensity of manual interventions for these individuals.

Although chiropractors report adapting their treatments based on age and perceived physical condition, the specific clinical and contextual factors influencing these therapeutic decisions remain poorly understood (Caissy et al., 2024). Perceived patient frailty, body type, and the chiropractor's own clinical experience may all play a role in guiding these choices. Furthermore, while it is assumed that adaptations in technique reflect a reduction in applied force, it is not yet established whether such adjustments result in measurable changes in treatment intensity compared to care provided to younger adults.

This observational study aims to address this gap by examining the factors that influence chiropractors' therapeutic decision-making when delivering manual therapies to both adult and aging patients. In parallel, it will assess whether clinical adaptations are associated with measurable differences in the force applied during treatment.

The primary objective is to identify clinical and contextual factors that influence chiropractors' therapeutic choices, especially when treating patients perceived as frail. The secondary objective is to compare the force applied during manual therapies between two age groups-patients aged 50 and older (aging group) and those aged 18-49 (younger adult group)-to determine if perceived adaptations correspond to actual reductions in applied force.

Hypotheses:

  • Chiropractors will adjust their therapeutic choices based on clinical factors indicative of patient frailty, such as age, medical history, physical condition, and clinical presentation.
  • The more fragile a patient is perceived to be (evaluated by the Pictorial Fit-Frail Scale and the Clinical Frailty Scale), the more likely the chiropractor will choose techniques considered safer and lower in applied force.
  • On average, the force applied during manual therapy will be lower for aging patients compared to younger adults.

Study Design and Procedures:

This study will be conducted in real-world clinical settings in Quebec. The chiropractor is the primary study participant, with the patient acting as a contextual intermediary, receiving their usual care. No modifications to clinical judgment or treatment type will be imposed.

Chiropractors who consent to participate will meet with the lead researcher to review study objectives, data collection procedures, and informed consent procedures. The discussion will help integrate the study into the clinical workflow with minimal disruption. During the data collection day, the chiropractor will treat patients as usual. A researcher will be present to observe the session and place a force sensor beneath the patient if applicable, depending on the treatment type. After each treatment, the chiropractor will complete a short questionnaire (<10 minutes) about the session. At the end of the day, a brief review and clarification session with the researcher (~10 minutes).

Patients will have been informed in advance (via phone, prior visit, or reception staff) that a research project may be taking place during their upcoming visit. On the day of data collection, they will have access to an information sheet and may ask questions before giving informed consent. If they agree, they will receive their usual care, with the presence of a researcher during treatment. A force sensor may be placed under them, depending on the nature of the manual therapy. Participation may add 5-10 minutes to their normal visit duration. Patients will complete a brief 5-question questionnaire either before or after the treatment.

This protocol is designed to minimize disruption to clinical routines. Observing patient care in a natural setting is essential to collecting contextual and force-related data.

The results of this study will provide new insights into clinical reasoning and force modulation during chiropractic care for aging patients. These findings may inform the development of future clinical guidelines aimed at improving both safety and effectiveness of manual therapy in older adults.

Data Analysis : Descriptive statistics will be used to report sample characteristics of both chiropractors and patients. Manual therapy force (measured in Newtons) will be calculated using a MATLAB script developed by the research team, which identifies the peak force manually for each intervention.

To explore the factors influencing chiropractors' therapeutic choices (e.g., spinal manipulation, mobilization, instrument-assisted techniques, use of blocks), a Bayesian statistical approach will be employed. This method allows for the direct estimation of the probability of various predictor effects (e.g., patient age, gender, frailty score, height, weight), while accounting for inter-practitioner variability.

Keywords
Aging, manual therapy, safety, chiropractic

What participants receive

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

Study groups in NCT07023809
Study groupRoleWhat they receive
ChiropractorsAll recruited chiropractors will be part of the same participant group. For each chiropractor, we plan to assess between 4 and 10 patients. Our goal is to analyze differences between the "younger" adult population (ages 18 to 49) and the "aging" adult population (ages 50 and older) in the context of care provided by each chiropractor.

What is being measured

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

  1. Care approaches

    The researcher will take handwritten notes of all spinal manual therapies performed by the chiropractors on their patients during the data collection day.

    Measured: From the start of the clinician work day to the end of the clinician work day (1 day)

Secondary outcomes (1)
  1. Manual therapy force

    For manual therapy delivered by the chiropractor with the patient lying prone and using a posteroanterior vector, a sensor will be placed between the chiropractor's contact point and the patient's skin. The peak force applied will be measured.

    Measured: From the start of the clinician work day to the end of the clinician work day (1 day)

Timeline

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

  1. First posted17 Jun 2025
  2. Study start1 Aug 2025
  3. Primary completion15 Dec 2025
  4. Study completion15 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
Cross-sectional
Enrolment
12 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07023809
Sponsor's protocol ID
UQTR_IP_Aging_2025
Status last verified
Jun 2026
First submitted
1 Jun 2025
Last updated
8 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: We plan to use Borealis, the institutional data repository at the university, for storing our IPD. This platform will ensure the long-term preservation of the data, facilitate its discovery, and manage controlled access. Borealis is freely accessible to project staff and offers multiple features to support secure data storage, sharing, and compliance with ethical standards.

Publications

  • Caissy, D., Brousseau, D., Blanchette, M. A., Grenier, J.-M. & Pagé, I. Étude descriptive de l'expérience des chiropraticiens lors du traitement des patients vieillissants. Mémoire de maîtrise thesis, Montréal ; Trois-Rivières, Université de Montréal ; Université du Québec à Trois-Rivières., (2024).

  • Hawk C, Schneider M, Dougherty P, Gleberzon BJ, Killinger LZ. Best practices recommendations for chiropractic care for older adults: results of a consensus process. J Manipulative Physiol Ther. 2010 Jul-Aug;33(6):464-73. doi: 10.1016/j.jmpt.2010.06.010.

    PubMed 20732584

Questions about this trial

What is this clinical trial studying?

An observational study of Muskuloskeletal Diseases, run by Université du Québec à Trois-Rivières at 1 site in Canada.

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 5 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 8 Jun 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 Canada. 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?

Care approaches (time frame: From the start of the clinician work day to the end of the clinician work day (1 day)). 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 NCT07023809, which also lists 2 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 8 Jun 2026.

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