CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 952 enrolled
Drug / intervention
RE-ACTIVE +2 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03455608
NCT03455608N/ACompleted

PRO-ACTIVE: Comparing The Effectiveness of Prophylactic Swallow Intervention for Patients Receiving Radiotherapy for Head and Neck Cancer

University Health Network, Toronto·interventional·Posted Mar 6, 2018·Updated Dec 10, 2024

In Brief

A clinical study evaluating RE-ACTIVE, PRO-ACTIVE EAT, and 1 other intervention for Dysphagia. Completed, enrolled 952 participants across 13 sites in 2 countries.

Detailed Summary

Dysphagia (difficulty swallowing) is a common and potentially life-threatening toxicity of radiotherapy (RT) for patients with head and neck cancer (HNC). HNC survivors have a 20-24 percent lifetime risk of pneumonia after RT, which is associated with a 42 percent excess risk of death in survivorship. Moreover, dysphagia predisposes individuals to malnutrition, and at least half of HNC patients require feeding tubes during RT. Patients are commonly referred for swallowing therapy with a speech pathologist. Some patients receive early intervention, before a swallowing problem begins-PRO-ACTIVE therapy. Other patients are monitored and prescribed dysphagia interventions only if and when a swallowing problem occurs-RE-ACTIVE therapy. Thus, REACTIVE therapy aims to reverse an already impaired swallowing ability, whereas PRO-ACTIVE therapy aims to prevent or reduce severity of dysphagia. These two broad categories of therapy represent the most common types of intervention offered to HNC patients across North America. Although there is single-institution evidence to support each practice, it is yet unknown which is most effective. To address this gap, the primary aim of this international, multi-site 3-arm pragmatic randomized clinical trial is to compare the effectiveness of PRO-ACTIVE (high and low intensity) versus RE-ACTIVE swallowing therapy among 952 patients with HNC planning to undergo RT, using duration of feeding tube dependence after RT as the primary outcome. Our secondary aim proposes to compare the relative benefit or harm of these swallowing interventions on secondary outcomes considered relevant to our stakeholder partners.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDysphagia
CountriesCanada, United States

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedMar 6, 2018
Enrollment StartSep 27, 2018
Primary CompletionNov 15, 2024
TodayJul 2, 2026
Enrollment to primary: 6.1 yearsPosted 8.3 years ago

Interventions

RE-ACTIVEbehavioral

Reactive intervention started promptly if/when dysphagia is identified

PRO-ACTIVE EATbehavioral

Early low intensity proactive intervention started before RT commences

PRO-ACTIVE EAT + EXERCISEbehavioral

Early high intensity proactive intervention started before RT commences