Default Options to Reduce Unnecessary Daily Imaging During Palliative Radiation

University of Pennsylvania

Status: Completed

Conditions: Cancer

Treatments: Behavioral: Default initiation

Study type: Interventional

Funder types: Other

Identifiers

NCT03110692

826810

Details and patient eligibility

About

The goal of this study is to reduce preference sensitive, unnecessary daily imaging during radiation treatment in which a pre-planned quality improvement default option for radiation treatment prescriptions will be introduced throughout the network of Penn Radiation Oncology.

Full description

The goal of this study is to reduce preference sensitive, unnecessary daily imaging during radiation treatment in which a pre-planned quality improvement default option for radiation treatment prescriptions will be introduced throughout the network of Penn Radiation Oncology. This study is a prospectively designed, observational trial with two comparison groups: (1) a usual practice group (control group) and (2) a default radiation treatment prescription group (intervention group), in which the usual practice group will subsequently rollover from control to intervention so that all sites and physicians in the practice network of Penn Radiation Oncology are exposed to intervention. The purpose of this study is to reduce preference sensitive, unnecessary daily imaging during radiation treatment with the implementation of a quality improvement initiative within 5 sites of Penn Radiation Oncology. We aim to leverage the introduction of a default prescription option to reduce the use of daily imaging in palliative intent cases where it has limited clinical benefit and adds to cost burden. Our objective is to encourage more patient-centric clinical practice.

Enrollment: 1,188 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Radiation treatment courses with palliative intent
• Palliative treatment of bone, soft tissue, and intracranial metastases
• Photon radiation with 3D conformal therapy (3DCRT) only

Exclusion criteria

• Use of intensity modulated radiation (IMRT) or stereotactic body radiation (SBRT) as radiation treatment modality
• Retreatment to same site
• Proton radiation

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

---

1,188 participants in 2 patient groups

Usual practice (control)

No Intervention group

Description:

The usual practice group will rollover to the intervention arm after 3 months.

Intervention

Experimental group

Description:

Default initiation: Introduce a default prescription template in the palliative setting in order to reduce unnecessary daily image guided radiation.

Treatment:

Behavioral: Default initiation