PROMs To Improve Care- Standardized vs Patient Specific
NCT ID: NCT04027569
Last Updated: 2025-04-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
NA
INTERVENTIONAL
2040-11-30
2040-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Outcome After Plate Osteosynthesis of Proximal Humerus Fractures Using Continous Passive Motioning Therapy
NCT05952622
An Osseoanchored Percutaneous Prosthesis Study Evaluating Stable Neural Signal Transmission in Subjects With Transhumeral Amputations
NCT03957226
Comparison of Prosthetic Assessment Tools and Factors Influencing the Outcome
NCT03329326
Rehabilitation With or Without Static Progressive Splinting for Wrist Stiffness
NCT01618227
Return of Function and External Rotation Post Proximal Humerus Fracture Fixation With Neutral Rotation Brace
NCT02073695
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
PSFS group
Patients in this arm will complete the patient specific functional scale (PSFS) during their visits
Patient Specific Functional Scale
A validated patient reported outcome measure that asks patients to write down activities and score them 0 to 10.
PROMIS PF group
Patients in this arm will complete the PROMIS Physical Function during their visits
PROMIS PF
A computer adaptive, validated patient reported outcome measure that measures physical function on a 1 to 100.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Patient Specific Functional Scale
A validated patient reported outcome measure that asks patients to write down activities and score them 0 to 10.
PROMIS PF
A computer adaptive, validated patient reported outcome measure that measures physical function on a 1 to 100.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Months
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Stanford University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Robin Kamal
Assistant Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Robin N Kamal, MD MBA
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
52021
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.