Survivorship Care Plan-Personal Health Record (SCP-PHR) for Cancer Survivors
This study is testing an online tool called the Survivorship Care Plan-Personal Health Record (SCP-PHR). This tool is designed to help cancer survivors manage their care after treatment. We want to see how well the SCP-PHR works and how easy it is for people to use. You might be able to join if you are 18 or older, have regular internet access, and were diagnosed with stage I, II, or III colon or rectal cancer and have finished your initial treatment. We will measure how well people follow recommendations for colorectal cancer surveillance (checking for cancer recurrence) after 12 months. The study is currently unclear on its recruitment status and plans to enroll 250 participants.
- Study design
- This study is an interventional trial, meaning participants will receive a specific intervention. It is a hybrid effectiveness-implementation trial, including a randomized clinical trial component.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for colorectal cancer surveillance outcomes, measured at 12 months.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Survivorship Plan HEalth REcord (SPHERE) Implementation Trial
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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What this trial measures
- Colorectal Cancer Surveillance Outcomes12 months
The CRC Surveillance Index (SI) will be extracted from the electronic medical record. For each observation period, every person-month is classified as either "covered" (eligible for the test during the month and covered) or "uncovered" (eligible for the test, but not covered). If a surveillance test (S) is delivered to an eligible patient at a particular time, then all person-months for the following recommended interval fall under a period of coverage (P1). If it is not renewed, then an uncovered portion of the observation period (U) is created. Further, if a second surveillance test (S2) is performed after some uncovered interval (U), additional covered months (P2) may be present during the observation period. For each patient, SI=100\*\[(P1+P2)/(P1+P2+U)\] for each surveillance test.