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Feasibility of Prospective Surveillance and Early Physical Therapy for Trismus

Feasibility of PRospective Surveillance and Early PhysiCal Therapy for TrIsmuS in Individuals With Head and Neck CancEr: A Single-Group Feasibility Trial (PRECISE)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06531083
Acronym
PRECISE
Enrollment
30
Registered
2024-07-31
Start date
2025-03-01
Completion date
2026-09-30
Last updated
2026-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and Neck Cancer, Trismus

Keywords

Physical Therapy

Brief summary

Trismus, or restricted jaw movement, can occur in individuals with head and neck cancer (HNC) undergoing surgery or radiation therapy. There is a paucity of research examining interventions for trismus. We aim to assess the feasibility of prospective surveillance and early intervention to mitigate trismus in individuals undergoing HNC treatment. Method: The investigators will conduct a pilot single group feasibility study involving 30 individuals with HNC who will be undergoing radiation therapy. Participants will be identified at the HNC new patient clinic. Participants will be seen weekly during radiation therapy and will receive early intervention including manual therapy and a device-based jaw exercise regimen if presenting with 5% or greater reduction in jaw opening compared to pre-treatment. The investigators will assess recruitment and completion rates, intervention acceptability, and data collection procedures. Descriptive statistics will summarize feasibility metrics and participant demographics. Findings will inform the design of a larger multicentre trial.

Detailed description

1. Background and rationale : Head and neck cancers (HNCs) originate in the nasal cavity, sinuses, lips, mouth, salivary glands, throat, and larynx. Individuals undergoing treatment for HNC often develop side effects such as oral mucositis xerostomia and experience difficulties with swallowing and speech. Along with these side effects, individuals with oral and oropharyngeal cancers can develop trismus, defined as restricted mouth opening (\< 35mm).The beneficial effects of early physical therapy programs in mitigating the incidence of trismus have not yet been fully established, and there are no validated protocols or guidelines regarding exercise therapy. The findings of this study will be crucial in developing effective rehabilitation strategies for patients with HNC and also will contribute to the development of tailored exercise programs and rehabilitation protocols, enabling physical therapists specifically to deliver personalized care for individuals with HNC. 2. Research question and Objectives : i. To evaluate the feasibility of a prospective surveillance approach for the early detection of trismus in patients with HNC. ii. To determine the acceptability of implementing an early physical therapy intervention which includes jaw and neck exercises, manual therapy for the jaw, and the use of a jaw device for managing trismus in individuals with HNC. 3. Methodology : This feasibility two-phase study will recruit individuals with HNC, who are undergoing or have completed radiotherapy. Phase I includes two cohorts: (1) a prospective surveillance cohort of individuals undergoing radiotherapy who are at risk of developing trismus, and (2) a post-radiotherapy cohort of individuals with established trismus. In the surveillance cohort, PT will be initiated if jaw mobility declines by \>5% relative to pre-treatment baseline or reaches a threshold of ≤35 mm. Participants in the post-radiotherapy cohort with established trismus (Mouth Opening (MO) ≤35 mm) will receive PT at enrolment. The intervention will include MT and therapeutic exercise. Phase II includes a qualitative assessment of the study's acceptability and delivery. The primary outcome is feasibility, including recruitment, adherence, and completion rates. Changes in MO will be explored descriptively as a secondary outcome. Participants will be identified at the HNC new patient clinic. Participants will receive early intervention including manual therapy and a device-based jaw exercise regimen if presenting with 5% or greater reduction in jaw opening compared to pre-treatment. Phase II includes a qualitative assessment of the study's acceptability and delivery. The primary outcome is feasibility, including recruitment, adherence, and completion rates. Changes in MO will be explored descriptively as a secondary outcome.

Interventions

Physical therapy including manual therapy, home exercises for the neck and jaw, and use of a jaw stretching device.

Sponsors

University of Alberta
Lead SponsorOTHER
Alberta Health services
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Prospective surveillance with early intervention

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Have a diagnosis of oral, oropharyngeal, or nasopharyngeal cancer * Be scheduled to undergo cancer treatment that includes radiation therapy * Be able to read and understand English * Be an Alberta resident.

Exclusion criteria

* Previous surgery for the temporomandibular joint that is not related to the HNC diagnosis. * Local cancer recurrence or metastatic disease. * Unable to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Feasibility: completion rate2 yearsNumber of participants completing the study.

Secondary

MeasureTime frameDescription
Feasibility: recruitment rate2 yearsNumber of participants entering the study by the number of participants eligible.
Feasibility: adherence rate6 weeks.Percentage of sessions completed over the 6-week intervention period.
Maximal interincisal opening3 monthsThe distance from the incisal border of tooth #21 to the middle of incisal border of tooth #31
Trismus symptom questionnaire3 monthsRevised Gothenburg Trismus Questionnaire (0-100): higher scores indicate higher symptom burden
Quality of life related to Head and Neck Cancer3 monthsUniversity of Washington Quality of Life scale (scored 0 to 100): higher scores indicate better functioning.
Cervical range of motion3 monthsQuantification of neck range of motion: higher scores reflect better function
Neck Disability3 monthsNeck Disability Index (0-50): higher scores reflect more disability
Intervention effect on health status6 weeksGlobal rating of change scale (VAS -7 to +7)

Countries

Canada

Contacts

CONTACTMargaret McNeely, PhD
mmcneely@ualberta.ca780-492-6007
CONTACTLynn Mohamad, PhDc
frmace@ualberta.ca780-492-6007
PRINCIPAL_INVESTIGATORMargaret McNeely, PhD

University of Alberta

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 13, 2026