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RecruitingNCT07283653Updated Feb 10, 2026

Dissemination and Implementation of DIGEST™ as an Evidence-based Measurement Tool for Dysphagia: A Randomized Implementation Trial

An interventional study of No intervention and DIGEST Training Program in DIGEST, Evidence Based Measurement and Dysphagia, sponsored by M.D. Anderson Cancer Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-10.

Sponsored by M.D. Anderson Cancer Center · Not applicable, Interventional, and Diagnostic

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Jun 2025, registered Dec 2025).
  • Started Jun 2025; still recruiting 1 year 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
85
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

To improve swallowing outcomes in cancer through clinical implementation of the Dynamic Imaging Grade of Swallowing Toxicity (DIGEST™) as an evidence-based practice (EBP) tool to grade pharyngeal dysphagia (difficulty swallowing) as a toxicity of cancer.

Read the detailed description

Primary Objective Assess the impact of implementation strategies on clinical adoption (reach) of DIGEST for oncology MBS studies.

Secondary Objective Assess the impact of implementation strategies on the fidelity (reliability) of DIGEST adoption for oncology MBS studies

02

Conditions studied

  • DIGEST
  • Evidence Based Measurement
  • Dysphagia
  • Randomized Implementation

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03

In context

Deglutition Disorders

710 studies on the registry are indexed under Deglutition Disorders; 219 are open to participants now.

This study's planned enrollment of 85 is above the median of 60 across 471 interventional studies indexed under Deglutition Disorders.

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Lead sponsor

M.D. Anderson Cancer Center is the lead sponsor of 2,999 studies on the registry; 581 are open to participants now.

Of its 599 completed or terminated interventional studies of FDA-regulated products, 402 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. A hospital or clinic affiliated with the Veteran's Affairs system, University of Wisconsin system, or Ohio State University system.
  2. A minimum average of 10 Modified Barium Swallow (MBS) procedures per month in oncology patients in preceding year.
  3. MBS imaging files are recorded and archived as a routine procedure (and accessible to researchers).

Exclusion criteria

Exclusion Criteria:

N/A

05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
85 participants (estimated)

Study arms

  • Experimental
    Control Arm 1

    The control arm will receive no active implementation strategy.

    Other: No intervention

  • Experimental
    Training Arm 2

    Represents a low intensity implementation strategy solely using the DIGEST training program as the intervention.

    Other: DIGEST Training Program

  • Experimental
    Training + Practice Facilitation Arm 3

    Represents a higher intensity strategy using the same training program plus practice facilitation.

    Other: DIGEST Training + Practice Facilitation

Interventions

  • OtherNo intervention

    receive no active implementation

  • OtherDIGEST Training Program

    Investigator led training program

  • OtherDIGEST Training + Practice Facilitation

    Training plus practice facilitation

06

What researchers measure

Primary outcomes

  1. Adoption of DIGEST in routine clinical documentation for oncology MBS studies

    Time frame: Through study completion; an average of 1 year

07

Study locations

1 of 1 sites recruiting
  • MD Anderson Cancer Center
    Houston, Texas 77030, United States
    • Kate Hutcheson, PHD · Contact · karnold@mdanderson.org · 713-792-6513
    • Kate Hutcheson, PHD · Principal investigator
    Recruiting
08

References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07283653
Lead sponsor
M.D. Anderson Cancer Center
Responsible party
Sponsor
First posted
Dec 16, 2025
Start date
Jun 1, 2025
Primary completion
Aug 1, 2027 (estimated)
Completion
Jan 31, 2029 (estimated)
Last update
Feb 10, 2026

Study contacts

Kate Hutcheson, PHD
Contact
karnold@mdanderson.org
713-792-6513
Kate Hutcheson, PHD
principal investigator · M.D. Anderson Cancer Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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