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NCT06989489 · ClinicalTrials.gov registry record · NA

Implementation of an Oral Chemotherapy Adherence Intervention

A NA study of Solid Tumor and Hematologic Malignancy, sponsored by UNC Lineberger Comprehensive Cancer Center.

Recruiting
Registry status
NA
Development phase
160
Enrollment target
1
Study location

NCT06989489: Recruiting NA study of Solid Tumor and Hematologic Malignancy, sponsored by UNC Lineberger Comprehensive Cancer Center.

NCT06989489 is a NA study of Solid Tumor and Hematologic Malignancy that is actively recruiting participants, run by UNC Lineberger Comprehensive Cancer Center. The registered enrollment target is 160 participants, below the 221-participant average among 196 other Solid Tumor trials with a reported enrollment target (28% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06989489, a NA study of Solid Tumor and Hematologic Malignancy, is actively recruiting participants, sponsored by UNC Lineberger Comprehensive Cancer Center.

RECRUITING
Registry status
NA
Development phase
160 participants
Enrollment target
1
Study location

Study Summary

The goal of this study is to evaluate the effectiveness and usability of a newly developed oral anticancer agent adherence program implemented across 6 cancer clinics (two academic, two urban, and two rural). The study will include 160 adult participants with either solid tumors or hematologic malignancies who have been taking oral anticancer agents for at least six months. This study will have two groups of participants, a pre- and post-implementation group. In the pre-implementation of the program group, investigators will administer a survey to the 80 participants and gather information about their medication prior to their enrollment of the program. Similarly, 80 participants who have been enrolled into this program for at least 6 months will serve as the post-implementation group. These patients will be administered the same survey. The results from both groups will be analyzed to see how effective the medication adherence program is.

Primary Outcome

Patient's medication adherence of their oral anticancer regiment will be quantified using the PROMIS- medication adherence Likert-type questionnaire, from strongly disagree to strongly agree. Score will change from 1 to 5, with a maximum of 50 and minimum of 10. A higher score reflects better adherence. These answers will help the investigators see if the program was effective in helping the patient's medication adherence.

Interventions

  • BEHAVIORAL Multilevel Adherence Intervention

Study Locations (1)

North Carolina

  • UNC Chapel Hill - Chapel Hill

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2025-05-28
Est. Completion 2028-08-30
Phase NA

What NCT06989489 shows while recruiting

NCT06989489 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, below the 221-participant average among 196 other Solid Tumor trials with a reported enrollment target (28% lower).

The record links to 2 conditions, with Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which Multilevel Adherence Intervention is the first listed.

NCT06989489 reports a single indexed study location in North Carolina.

Frequently Asked Questions

What is clinical trial NCT06989489 about?

NCT06989489 is a clinical study titled "Implementation of an Oral Chemotherapy Adherence Intervention". The goal of this study is to evaluate the effectiveness and usability of a newly developed oral anticancer agent adherence program implemented across 6 cancer clinics (two academic, two urban, and two rural). The study will include 160 adult participants with either solid tumors or hematologic malig...

What is the current status of trial NCT06989489?

This trial is currently recruiting. It is a NA study. The enrollment target is 160 participants. The study started on 2025-05-28. Estimated completion is 2028-08-30.

What conditions does trial NCT06989489 study?

This clinical trial studies the following conditions: Solid Tumor, Hematologic Malignancy.

What interventions are being tested in trial NCT06989489?

The interventions under investigation include: Multilevel Adherence Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT06989489?

This trial is sponsored by UNC Lineberger Comprehensive Cancer Center, which has 366 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06989489 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Solid Tumor

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06989489's enrollment target sits among peer trials

160 55th of 196 higher than 141 of 196 other Solid Tumor trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Solid Tumor trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06989489, the US trial registry maintained by the National Library of Medicine. NCT06989489 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.