{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Quality+of+Life+Supportive+Resources", "query": { "intervention": "Quality of Life Supportive Resources" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 74, "total_pages": 8, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Quality+of+Life+Supportive+Resources&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-12T22:03:56.609Z", "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": "NCT01126346", "title": "Quality of Life and Survivorship Care in Patients Undergoing Hyperthermic Intraperitoneal Chemotherapy (HIPEC)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Advanced Malignant Mesothelioma", "Carcinoma of the Appendix", "Ovarian Sarcoma", "Ovarian Stromal Cancer", "Pseudomyxoma Peritonei", "Recurrent Colon Cancer", "Recurrent Malignant Mesothelioma", "Recurrent Ovarian Epithelial Cancer", "Recurrent Ovarian Germ Cell Tumor", "Stage III Colon Cancer", "Stage III Ovarian Epithelial Cancer", "Stage III Ovarian Germ Cell Tumor", "Stage IV Colon Cancer", "Stage IV Ovarian Epithelial Cancer", "Stage IV Ovarian Germ Cell Tumor", "Unspecified Childhood Solid Tumor, Protocol Specific" ], "interventions": [ { "name": "HIPEC Orientation", "type": "BEHAVIORAL" }, { "name": "Consultation with Survivorship Navigator", "type": "BEHAVIORAL" }, { "name": "Questionnaires", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 10, "start_date": "2010-05", "completion_date": "2013-10", "has_results": false, "last_update_posted_date": "2018-07-03", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01126346" }, { "nct_id": "NCT07250061", "title": "Self-Help Cognitive Processing Therapy (CPT)/Women Veterans Network (WoVeN) Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Posttraumatic Stress Disorder", "Depression" ], "interventions": [ { "name": "Self-Help Cognitive Processing Therapy", "type": "BEHAVIORAL" }, { "name": "Women Veterans Network (WoVeN)", "type": "BEHAVIORAL" }, { "name": "Treatment as Usual", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Boston 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": 100, "start_date": "2026-03-05", "completion_date": "2028-03", "has_results": false, "last_update_posted_date": "2026-05-27", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07250061" }, { "nct_id": "NCT05369429", "title": "My Wellbeing Guide: A Novel Tool for Managing Stress and Improving Quality of Life", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Anxiety", "Depressive Symptoms" ], "interventions": [ { "name": "My Wellbeing Guide", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6516, "start_date": "2022-12-02", "completion_date": "2028-07-05", "has_results": false, "last_update_posted_date": "2026-06-01", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05369429" }, { "nct_id": "NCT06853925", "title": "Testing a Web-based Intervention for Radioactive Iodine Symptom Management to Improve Health-related Quality of Life Among Differentiated Thyroid Cancer Patients", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Thyroid Neoplasms" ], "interventions": [ { "name": "Radioactive Iodine Support (RAI Support)", "type": "BEHAVIORAL" }, { "name": "Treatment as Usual (TAU)", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Georgetown University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 88, "start_date": "2025-10-02", "completion_date": "2027-02", "has_results": false, "last_update_posted_date": "2026-01-16", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06853925" }, { "nct_id": "NCT03998618", "title": "Telephone Support for Metastatic Breast Cancer Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Metastatic Breast Cancer" ], "interventions": [ { "name": "Acceptance and Commitment Therapy", "type": "BEHAVIORAL" }, { "name": "Education/Support", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Indiana 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": 250, "start_date": "2019-06-20", "completion_date": "2023-09-13", "has_results": true, "last_update_posted_date": "2024-10-10", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 3, "location_summary": "Chicago, Illinois • Indianapolis, Indiana", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT03998618" }, { "nct_id": "NCT06557863", "title": "Reducing Burden in Care Partners of Community-Dwelling Persons With Dementia and Oropharyngeal Dysphagia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Caregiver Burden", "Alzheimer Disease", "Dementia", "Oropharyngeal Dysphagia" ], "interventions": [ { "name": "WeCareToFeedDysphagia web tool", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 80, "start_date": "2024-10-08", "completion_date": "2025-08-01", "has_results": true, "last_update_posted_date": "2026-06-01", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06557863" }, { "nct_id": "NCT03938324", "title": "Peer i-Coaching for Activated Self-Management Optimization in Adolescents and Young Adults With Chronic Conditions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sickle Cell Disease", "Chronic Kidney Diseases", "Systemic Lupus Erythematosus", "Childhood Cancer", "Inflammatory Bowel Diseases", "Stem Cell Transplant", "Organ Transplant", "Diabetes Mellitus, Type 1", "Cystic Fibrosis" ], "interventions": [ { "name": "PiCASO Intervention Group", "type": "BEHAVIORAL" }, { "name": "Sham Comparator: Attention Control Group", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "16 Years", "maximum_age": "22 Years", "sex": "ALL", "summary": "16 Years to 22 Years" }, "enrollment_count": 222, "start_date": "2019-10-29", "completion_date": "2024-06-19", "has_results": true, "last_update_posted_date": "2026-07-17", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03938324" }, { "nct_id": "NCT04330365", "title": "Pragmatic Trial of WHT vs. PC-GE to Promote Non-Pharmacological Strategies to Treat Chronic Pain in Veterans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Pain" ], "interventions": [ { "name": "Whole Health Team (WHT) Intervention Arm, Primary Care Group Education (PC-GE) Intervention Arm, Usual Primary Care (UPC) Arm", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "San Francisco Veterans Affairs Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 793, "start_date": "2020-09-15", "completion_date": "2025-01-23", "has_results": true, "last_update_posted_date": "2026-06-02", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 6, "location_summary": "San Francisco, California • West Haven, Connecticut • Tampa, Florida + 3 more", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "West Haven", "state": "Connecticut" }, { "city": "Tampa", "state": "Florida" }, { "city": "Bedford", "state": "Massachusetts" }, { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04330365" }, { "nct_id": "NCT06123988", "title": "Prolonged Overnight Fasting and/or Exercise on Fatigue and Other Patient Reported Outcomes in Women With Hormone Receptor Positive Advanced Breast Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HER2-positive Breast Cancer", "Advanced Breast Cancer" ], "interventions": [ { "name": "Prolonged Overnight Fasting", "type": "BEHAVIORAL" }, { "name": "Moderate-Intensity Exercise", "type": "BEHAVIORAL" }, { "name": "General Health Education Sessions", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Miami", "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": 260, "start_date": "2024-09-09", "completion_date": "2029-09-30", "has_results": false, "last_update_posted_date": "2026-08-26", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 3, "location_summary": "Phoenix, Arizona • Miami, Florida • Boston, Massachusetts", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Miami", "state": "Florida" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06123988" }, { "nct_id": "NCT07071038", "title": "Evaluating the Use of a Medication 'Switch' vs Guideline-directed Interventions for Relieving Side Effects of Aromatase Inhibitors Among Breast Cancer Patients", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Breast Cancer", "Adjuvant Treatment", "Early Stage Breast Cancer" ], "interventions": [ { "name": "Switch", "type": "DRUG" }, { "name": "Guideline Directed Intervention (GDI)", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Dartmouth-Hitchcock Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 62, "start_date": "2025-10-17", "completion_date": "2027-08-05", "has_results": false, "last_update_posted_date": "2026-02-12", "last_synced_at": "2026-09-12T22:03:56.609Z", "location_count": 1, "location_summary": "Lebanon, New Hampshire", "locations": [ { "city": "Lebanon", "state": "New Hampshire" } ], "official_url": "https://clinicaltrials.gov/study/NCT07071038" } ] }