{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=2+Feet+4+Life", "query": { "intervention": "2 Feet 4 Life" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 12, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=2+Feet+4+Life&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-07T02:01:09.628Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT06591780", "title": "Innovative Multi-Variable Biofeedback for Improving Gait Performance in Individuals With Diabetic Peripheral Neuropathy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Peripheral Neuropathy", "Diabetes Mellitus" ], "interventions": [ { "name": "Clinical Evaluation", "type": "OTHER" }, { "name": "Plantar Pressure Biofeedback Gait Training", "type": "OTHER" }, { "name": "Propulsion Biofeedback Gait Training", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Florida Institute for Human and Machine Cognition", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "45 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "45 Years to 90 Years" }, "enrollment_count": 25, "start_date": "2025-10-20", "completion_date": "2027-06-01", "has_results": false, "last_update_posted_date": "2026-03-11", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Pensacola, Florida", "locations": [ { "city": "Pensacola", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06591780" }, { "nct_id": "NCT05419245", "title": "Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Freeman-Burian Syndrome", "Freeman-Sheldon Syndrome", "Whistling Face Syndrome", "Sheldon-Hall Syndrome", "Freeman-Sheldon Syndrome Variant", "Arthrogryposis Distal Type 1", "Arthrogryposis Distal Type 3", "Gordon Syndrome" ], "interventions": [ { "name": "Guided Health History for Freeman-Burian Syndrome Questionnaire", "type": "OTHER" }, { "name": "Freeman-Burian syndrome Semi-Structured Quality of Life Interview", "type": "OTHER" }, { "name": "Medical Records Review", "type": "OTHER" }, { "name": "PTSD Checklist for DSM-5", "type": "OTHER" }, { "name": "Modified Flanagan Quality of Life Scale", "type": "OTHER" }, { "name": "Center for Epidemiologic Studies Depression Scale", "type": "OTHER" }, { "name": "Review of Systems", "type": "OTHER" }, { "name": "FACE-Q | Craniofacial - Appearance of the Face", "type": "OTHER" }, { "name": "FACE-Q | Craniofacial - Appearance Distress", "type": "OTHER" }, { "name": "FACE-Q | Craniofacial - Facial Function", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Dufresne, Craig, MD, PC", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 20, "start_date": "2022-06-01", "completion_date": "2023-12", "has_results": false, "last_update_posted_date": "2022-07-19", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Fairfax, Virginia", "locations": [ { "city": "Fairfax", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05419245" }, { "nct_id": "NCT02658708", "title": "Bright Light on Fatigue in Women Being Treated for Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Breast Neoplasms", "Breast Cancer", "Cancer of Breast", "Cancer of the Breast" ], "interventions": [ { "name": "Bright blue-green light using light visor cap", "type": "OTHER" }, { "name": "Dim red light using light visor cap", "type": "OTHER" }, { "name": "European Organization for Research and Treatment of Cancer-Quality of Life Questionnaire", "type": "OTHER" }, { "name": "Epworth Sleepiness Scale", "type": "OTHER" }, { "name": "Pittsburgh Sleep Quality Index", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Sleep Disturbance", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Cancer-Fatigue", "type": "OTHER" }, { "name": "Digital foot candle datalogging light meter (Extech Instrument, Model SDL400)", "type": "DIAGNOSTIC_TEST" }, { "name": "Polysomnography (Easy Ambulatory 2 Cadwell, Kennewick, WA)", "type": "DIAGNOSTIC_TEST" }, { "name": "Horne-Ostberg Morningness-Eveningness Questionnaire", "type": "OTHER" }, { "name": "Daily Fatigue and Sleep Log", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 19, "start_date": "2015-10-12", "completion_date": "2017-05-09", "has_results": false, "last_update_posted_date": "2017-09-25", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02658708" }, { "nct_id": "NCT03656341", "title": "Foot Self-care in Older Adults", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Foot" ], "interventions": [ { "name": "2 Feet 4 Life", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Missouri-Columbia", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 32, "start_date": "2018-09-27", "completion_date": "2019-09-17", "has_results": false, "last_update_posted_date": "2019-10-25", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 2, "location_summary": "Broken Arrow, Oklahoma • Owasso, Oklahoma", "locations": [ { "city": "Broken Arrow", "state": "Oklahoma" }, { "city": "Owasso", "state": "Oklahoma" } ], "official_url": "https://clinicaltrials.gov/study/NCT03656341" }, { "nct_id": "NCT05965336", "title": "Walking Function in Diabetic Peripheral Neuropathy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Peripheral Neuropathy" ], "interventions": [ { "name": "Clinical Evaluation", "type": "OTHER" }, { "name": "Evaluation of Passive Ankle Stiffness", "type": "OTHER" }, { "name": "Gait Biomechanics", "type": "OTHER" }, { "name": "Gait Biofeedback", "type": "OTHER" }, { "name": "Plantar Pressure Biofeedback Gait Training", "type": "OTHER" }, { "name": "Propulsion Biofeedback Gait Training", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Florida Institute for Human and Machine Cognition", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": null, "sex": "ALL", "summary": "45 Years and older" }, "enrollment_count": 50, "start_date": "2024-12-05", "completion_date": "2027-08-31", "has_results": false, "last_update_posted_date": "2026-08-18", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Pensacola, Florida", "locations": [ { "city": "Pensacola", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05965336" }, { "nct_id": "NCT04258969", "title": "Pedaling at a Low-Moderate Intensity During Chemotherapy Administration", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colorectal Cancer", "Exercise, Aerobic", "Chemotherapy", "Chemotherapeutic Toxicity" ], "interventions": [ { "name": "Pedaling", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rush University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2020-01-11", "completion_date": "2021-10-14", "has_results": false, "last_update_posted_date": "2024-10-01", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04258969" }, { "nct_id": "NCT05926024", "title": "Long-Term Follow-Up in Women With Early Breast Cancer Three Years of More Post Primary Treatment", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Exercise Recall Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Health Behavior Questionnaire (HBQ)30 Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Functional Assessment of Cancer Therapy-General (FACT-G) Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PROMIS Cognitive Function (Short Form 8a)", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Functional Assessment of Cancer-Gynecology Oncology Group-Neurotoxicity (FACT/GOG-NTX-12)", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PROMIS", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes FACT-Endocrine Symptoms", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Penn Arthralgia Aging Survey", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PRO-CTCAE (patient-reported CTCAE)", "type": "BEHAVIORAL" }, { "name": "p16 tumor suppressor gene", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "BEHAVIORAL", "DIAGNOSTIC_TEST" ], "sponsor": "UNC Lineberger Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 253, "start_date": "2023-01-06", "completion_date": "2028-01-31", "has_results": false, "last_update_posted_date": "2026-03-11", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05926024" }, { "nct_id": "NCT01764035", "title": "Mindfulness Therapy on Disrupted Sleep in Bipolar Disorder", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bipolar Disorder", "Insomnia", "Hypersomnia", "Sleep Problems" ], "interventions": [ { "name": "Body Scan (BS) Meditation Intervention", "type": "BEHAVIORAL" }, { "name": "Brief Supportive Psychotherapy (SP)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 48, "start_date": "2013-02", "completion_date": "2016-02", "has_results": false, "last_update_posted_date": "2016-06-24", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01764035" }, { "nct_id": "NCT02221700", "title": "Massage Therapy in Reducing Chemotherapy-Induced Peripheral Neuropathy in Patients With Gastrointestinal or Breast Malignancies", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Malignant Breast Neoplasm", "Malignant Digestive System Neoplasm", "Peripheral Neuropathy" ], "interventions": [ { "name": "Massage Therapy", "type": "PROCEDURE" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 90, "start_date": "2015-04-09", "completion_date": "2027-04-30", "has_results": false, "last_update_posted_date": "2026-03-09", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02221700" }, { "nct_id": "NCT01243541", "title": "Cryotherapy in Preventing Peripheral Neuropathy and Nail Toxicity in Patients With Breast Cancer Who Are Receiving Paclitaxel", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chemotherapeutic Agent Toxicity", "Pain", "Peripheral Neuropathy", "Recurrent Breast Cancer", "Stage IA Breast Cancer", "Stage IB Breast Cancer", "Stage II Breast Cancer", "Stage IIIA Breast Cancer", "Stage IIIB Breast Cancer", "Stage IIIC Breast Cancer", "Stage IV Breast Cancer", "Therapy-related Toxicity" ], "interventions": [ { "name": "cryotherapy", "type": "PROCEDURE" }, { "name": "questionnaire administration", "type": "OTHER" }, { "name": "quality-of-life assessment", "type": "PROCEDURE" }, { "name": "management of therapy complications", "type": "PROCEDURE" }, { "name": "assessment of therapy complications", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 33, "start_date": "2010-11-03", "completion_date": "2014-04-04", "has_results": false, "last_update_posted_date": "2019-08-20", "last_synced_at": "2026-09-07T02:01:09.628Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT01243541" } ] }