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Study Title: Protocol Number: Version Number: Version Date: Replaces:A resistance training program to improve physical function in sarcoma survivors 19942 4.0 16 APR 2020 version 3.0, dated 10 MAR
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Begin by carefully reviewing the Knight Investigator-Initiated Trial Protocol template provided.
02
Fill out all relevant sections of the protocol, ensuring to provide detailed information about the study design, methodology, and objectives.
03
Clearly outline the inclusion and exclusion criteria for study participants.
04
Describe the procedures for recruitment, screening, and enrollment of participants.
05
Provide a detailed outline of the study interventions, including dosages, schedules, and any necessary monitoring.
06
Detail the methods for data collection, analysis, and reporting.
07
Include any necessary appendices, such as study forms or questionnaires.
08
Once the protocol is filled out, review it carefully to ensure all information is accurate and complete before submission.

Who needs knight investigator-initiated trial protocol?

01
Researchers and investigators who are planning to conduct a clinical trial under the Knight Investigator-Initiated Trial program would need to fill out this protocol.
02
Institutional review boards and regulatory authorities may also require this protocol for review and approval.
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Knight investigator-initiated trial protocol is a document outlining the details of a clinical trial that has been designed and initiated by an investigator, rather than by a sponsor.
The investigator who is leading the trial is required to file the knight investigator-initiated trial protocol.
The protocol is typically filled out by the investigator with details such as study objectives, methods, participant eligibility criteria, and study procedures.
The purpose of the protocol is to provide a clear outline of the trial design and procedures to ensure the safety of participants and the validity of the trial results.
The protocol must include details on study objectives, methods, participant eligibility criteria, study procedures, data analysis plan, and ethical considerations.
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