{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lifestyle+Modification+Intervention&page=2", "query": { "intervention": "Lifestyle Modification Intervention", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lifestyle+Modification+Intervention&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-25T01:31:57.732Z", "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": "NCT03535701", "title": "Ketogenic Diet and Chemotherapy in Affecting Recurrence in Patients With Stage IV Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Stage IV Breast Cancer AJCC v6 and v7" ], "interventions": [ { "name": "Dietary Intervention", "type": "DIETARY_SUPPLEMENT" }, { "name": "Laboratory Biomarker Analysis", "type": "OTHER" }, { "name": "Paclitaxel", "type": "DRUG" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER", "DRUG" ], "sponsor": "Ohio State University Comprehensive 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": 20, "start_date": "2017-10-20", "completion_date": "2020-05-01", "has_results": false, "last_update_posted_date": "2025-06-08", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03535701" }, { "nct_id": "NCT02342730", "title": "Weight Loss Referral for Healthier Survivorship in Obese Stage I-II Endometrial Cancer Survivors or Atypical Hyperplasia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Complex Endometrial Hyperplasia With Atypia", "Stage IA Uterine Corpus Cancer", "Stage IB Uterine Corpus Cancer", "Stage II Uterine Corpus Cancer" ], "interventions": [ { "name": "Weight Loss Specialist", "type": "BEHAVIORAL" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Medical Chart Review", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Case Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 127, "start_date": "2014-12-17", "completion_date": "2015-05-18", "has_results": false, "last_update_posted_date": "2018-11-19", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02342730" }, { "nct_id": "NCT06105957", "title": "Optimal Digital Weight Loss Treatment for Rural Individuals", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Overweight and Obesity" ], "interventions": [ { "name": "Core", "type": "BEHAVIORAL" }, { "name": "Facilitated Weekly Group Sessions", "type": "BEHAVIORAL" }, { "name": "Counselor Crafted Feedback", "type": "BEHAVIORAL" }, { "name": "Individual Coaching Calls", "type": "BEHAVIORAL" }, { "name": "Pre-Scripted Feedback", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 616, "start_date": "2024-01-03", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2025-12-23", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Columbia, South Carolina", "locations": [ { "city": "Columbia", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06105957" }, { "nct_id": "NCT06023576", "title": "A Study of Blood Pressure Control During Cancer Treatment", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Breast Cancer", "Cardiotoxicity" ], "interventions": [ { "name": "antihypertensive medications", "type": "OTHER" }, { "name": "Blood pressure measurement", "type": "DIAGNOSTIC_TEST" }, { "name": "Echocardiogram", "type": "DIAGNOSTIC_TEST" }, { "name": "Symptom-limited cardiopulmonary exercise test", "type": "OTHER" }, { "name": "Quality of Life Measures", "type": "OTHER" }, { "name": "Biomarkers", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "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": 130, "start_date": "2023-08-18", "completion_date": "2029-05-30", "has_results": false, "last_update_posted_date": "2026-05-14", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 7, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Montvale, New Jersey + 4 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06023576" }, { "nct_id": "NCT02564315", "title": "The Long-Term Quitting (Smoking Cessation) Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Smoking Cessation" ], "interventions": [ { "name": "Nicotine Mini-Lozenge for 11 Months", "type": "DRUG" }, { "name": "Preparation Phase Behavioral Reduction Counseling", "type": "BEHAVIORAL" }, { "name": "Preparation Phase Recycling Counseling", "type": "BEHAVIORAL" }, { "name": "Preparation Phase Control Treatment", "type": "BEHAVIORAL" }, { "name": "Cessation Phase Supportive Counseling", "type": "BEHAVIORAL" }, { "name": "Cessation Phase Skill Training Counseling", "type": "BEHAVIORAL" }, { "name": "Cessation Phase Brief Information", "type": "BEHAVIORAL" }, { "name": "Cessation Phase Nicotine Patch + Nicotine Mini-Lozenge", "type": "DRUG" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1154, "start_date": "2015-10-30", "completion_date": "2019-11-05", "has_results": false, "last_update_posted_date": "2020-02-17", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT02564315" }, { "nct_id": "NCT03749746", "title": "Heart Health 4 New Moms: A Randomized Trial in the First Year After Preeclampsia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Preeclampsia", "Gestational Hypertension", "Hypertension", "Obesity", "Overweight and Obesity", "Pregnancy Complications", "Pregnancy Toxemia", "Postpartum Preeclampsia" ], "interventions": [ { "name": "Home Blood Pressure Monitoring", "type": "BEHAVIORAL" }, { "name": "Heart Health 4 New Moms", "type": "BEHAVIORAL" }, { "name": "Usual care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 148, "start_date": "2019-01-26", "completion_date": "2021-12-01", "has_results": false, "last_update_posted_date": "2021-12-03", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03749746" }, { "nct_id": "NCT02963740", "title": "Feasibility of High Levels of Energy Expenditure From Physical Activity for Breast Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer Female" ], "interventions": [ { "name": "Supervised Exercise", "type": "BEHAVIORAL" }, { "name": "Home-based Exercise", "type": "BEHAVIORAL" }, { "name": "Group Phone Calls", "type": "BEHAVIORAL" }, { "name": "Diet", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Kansas Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "71 Years", "sex": "FEMALE", "summary": "Up to 71 Years · Female only" }, "enrollment_count": 11, "start_date": "2016-11", "completion_date": "2017-03", "has_results": false, "last_update_posted_date": "2022-01-25", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Kansas City, Kansas", "locations": [ { "city": "Kansas City", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02963740" }, { "nct_id": "NCT04559789", "title": "Reducing Dementia Risk With Digital Health Coaching", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alzheimer Disease", "Dementia", "Mild Cognitive Impairment", "Cognitive Decline" ], "interventions": [ { "name": "MindMate + Health Coaching", "type": "BEHAVIORAL" }, { "name": "Health Education", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Neurotrack Technologies, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "45 Years to 75 Years" }, "enrollment_count": 200, "start_date": "2021-01-04", "completion_date": "2024-01-30", "has_results": false, "last_update_posted_date": "2021-08-31", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Fayetteville, Arkansas", "locations": [ { "city": "Fayetteville", "state": "Arkansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04559789" }, { "nct_id": "NCT05012176", "title": "An Episodic Future Thinking Intervention to Promote Weight Loss in Breast Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anatomic Stage 0 Breast Cancer AJCC v8", "Anatomic Stage I Breast Cancer AJCC v8", "Anatomic Stage IA Breast Cancer AJCC v8", "Anatomic Stage IB Breast Cancer AJCC v8", "Anatomic Stage II Breast Cancer AJCC v8", "Anatomic Stage IIA Breast Cancer AJCC v8", "Anatomic Stage IIB Breast Cancer AJCC v8", "Anatomic Stage III Breast Cancer AJCC v8", "Anatomic Stage IIIA Breast Cancer AJCC v8", "Anatomic Stage IIIB Breast Cancer AJCC v8", "Anatomic Stage IIIC Breast Cancer AJCC v8", "Breast Ductal Carcinoma In Situ", "Invasive Breast Carcinoma", "Prognostic Stage 0 Breast Cancer AJCC v8", "Prognostic Stage I Breast Cancer AJCC v8", "Prognostic Stage IA Breast Cancer AJCC v8", "Prognostic Stage IB Breast Cancer AJCC v8", "Prognostic Stage II Breast Cancer AJCC v8", "Prognostic Stage IIA Breast Cancer AJCC v8", "Prognostic Stage IIB Breast Cancer AJCC v8", "Prognostic Stage III Breast Cancer AJCC v8", "Prognostic Stage IIIA Breast Cancer AJCC v8", "Prognostic Stage IIIB Breast Cancer AJCC v8", "Prognostic Stage IIIC Breast Cancer AJCC v8" ], "interventions": [ { "name": "Behavioral Intervention", "type": "BEHAVIORAL" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Ohio State University Comprehensive Cancer Center", "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": 50, "start_date": "2021-11-01", "completion_date": "2023-11-03", "has_results": false, "last_update_posted_date": "2025-02-07", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05012176" }, { "nct_id": "NCT01714271", "title": "Promotora-based Latino Family CVD Risk Reduction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Heart Disease", "Cancer" ], "interventions": [ { "name": "Home environs-based lifestyle counseling", "type": "BEHAVIORAL" }, { "name": "Cancer early detection", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 204, "start_date": "2010-10", "completion_date": "2014-10", "has_results": false, "last_update_posted_date": "2023-10-02", "last_synced_at": "2026-09-25T01:31:57.732Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01714271" } ] }