Clinical trials: Acceptability
HIV (Human Immunodeficiency Virus), Pain
Auricular Point Acupressure for Pain
The goal of this pilot clinical trial is to learn whether auricular point acupressure (APA) can help reduce chronic musculoskeletal pain in adults age 50 and older who are living with HIV.
- Trial name
- NCT07852611
- Testing
- Auricular Point Acupressure
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- Dan Song
Perceptions, Acceptability
Parental Perceptions and Acceptance of Silver Diamine Fluoride in Italy
Parental perceptions on staining due to Silver Diamine Fluoride (SDF) could affect its implementation in pediatric dentistry. This study represents the second part of a wider project focused on SDF aesthetic acceptability among…
- Conditions
- Perceptions, Acceptability, SDF
- Trial name
- SDF (NCT06300034)
- Where
- Italy
- Volunteers
- 234 people
- Sponsor
- University of Bologna
Hygiene
Dermacyd PH_DESILSTY_FR (Lactic Acid) - Acceptability - Stay on Frutal
Primary Objective: To prove the safety of the gynecological formulation in normal conditions of use.
- Trial name
- NCT00932945
- Testing
- LACTIC ACID(ND)
- Where
- Brazil
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- Sanofi
Smoking
User Acceptability of a Nicotine Lactate Delivery System (P3L)
This study will provide an initial assessment of the acceptability of the Nicotine Lactate Delivery System (P3L) after ad libitum use and the ability of combustible cigarette (CC) smokers to use P3L to maintain their customary…
- Trial name
- NCT02643693
- Testing
- P3L, VUSE, CC
- Where
- United States
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- Philip Morris Products S.A.
Feasibility, Acceptability
Air Purifiers in Classrooms for Infection Control - a Pilot Study
This study aims to investigate the acceptability and feasibility of deploying air purifiers equipped with HEPA (high-efficiency particulate air) filters in classrooms, to study air purifiers as an infection control measure.
- Trial name
- NCT06374316
- Testing
- Ceiling-Mounted Air Purifiers, Portable Air Purifiers, Portable or Ceiling Mounted Air Purifiers
- Where
- Norway
- Volunteers
- 6 people
- Sponsor
- Norwegian Institute of Public Health
Child Mortality, Azithromycin
Resiliency Through Azithromycin for Children (REACH), Côte d'Ivoire
The aim of the study is to gather preliminary evidence on the operational feasibility and acceptability of integrating bi-annual mass drug administration (MDA) of single-dose azithromycin for children ages 1 to 11 months in high…
- Trial name
- REACH (NCT04617626)
- Testing
- Azithromycin
- Where
- Côte d’Ivoire
- Volunteers
- 1,735 people, healthy volunteers welcome
- Sponsor
- FHI 360
Menstrual Health Intervention, Product Use Issue
An MHH Intervention in Bangladesh Health Systems
Over 50% of Bangladeshi women and girls use old cloths as menstrual absorbents due to cost, comfort, and familiarity. A substantial proportion, comprising 52% of adolescent girls and 62% of women washed the cloths with soap and…
- Conditions
- Menstrual Health Intervention, Product Use Issue, Hygiene Practices and Knowledge, Menstrual Hygiene Management
- Trial name
- NCT07723885
- Testing
- Menstrual health and hygiene intervention
- Where
- Bangladesh
- Volunteers
- 700 people, healthy volunteers welcome
- Sponsor
- International Centre for Diarrhoeal Disease Research, Bangladesh
Cystic Fibrosis
Evaluation of Patient Access to People With Cystic Fibrosis (CF) and Healthcare Professionals
Cystic fibrosis (CF) is one of the most common inherited conditions in the United Kingdom (UK). There are 10,810 people living with CF in the UK, with median predicted survival now 47 years old.
- Trial name
- NCT06122025
- Testing
- Patient Access
- Where
- United Kingdom
- Volunteers
- 102 people
- Sponsor
- The Leeds Teaching Hospitals NHS Trust
Feasibility, Acceptability
The TARANG Intervention
The mixed methods pilot study aims to evaluate the acceptability, feasibility, and implementation challenges of the TARANG intervention in villages in rural/tribal Rajasthan to inform the study design and operational details for…
- Conditions
- Feasibility, Acceptability, Family Planning, Unintended Pregnancy
- Trial name
- TARANGPilot (NCT06320964)
- Testing
- TARANG
- Where
- India
- Volunteers
- 42 people
- Sponsor
- University of California, San Francisco
Chronic Inflammatory Small Bowel Disease
Modified antioxIdants Bacteria for Gut Inflammation
Patients with IBD experience complex therapeutic pathways. The development of new treatments, more effective and free of side effects, is a therapeutic need.
- Trial name
- MOBIDIC (NCT06189599)
- Where
- France
- Volunteers
- 500 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Provoked, Localized Vulvodynia, Provoked Vestibulodynia
Provoked, Localized Vulvodynia Treatment With Acupuncture and Lidocaine Pilot Study
The investigators research project is a randomized, controlled, single-blinded, feasibility pilot study. The investigators will study the feasibility of a novel treatment for women with Provoked Localized Vulvodynia (PLV) with…
- Conditions
- Provoked, Localized Vulvodynia, Provoked Vestibulodynia, Vulvar Vestibulitis, Vulvodynia
- Trial name
- NCT01996384
- Testing
- Classical Acupuncture, Non-classical acupuncture, Lidocaine
- Where
- United States
- Volunteers
- 19 people
- Sponsor
- Oregon College of Oriental Medicine
Telemedicine
Evaluation of MHP 3.0 in Two Clinical Settings
The purpose of this study is to assess the acceptability and feasibility of the use of MyHealthyPregnancy (MHP) 3.0 in clinical practice over a 1 year period of time.
- Trial name
- NCT04863521
- Testing
- MHP
- Where
- United States
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- Naima Health LLC
Healthy, Breast Cancer
Validation of a Tear-based Screening Assay for Breast Cancer
This study will explore and better understand the value, usage, and benefits of a tear-based screening test for breast cancer as a supplemental tool for screening mammograms.
- Conditions
- Healthy, Breast Cancer, Breast Cancer Female, Health Care Utilization
- Trial name
- NCT04928014
- Testing
- Schirmer Strip
- Where
- United States
- Volunteers
- 205 people, healthy volunteers welcome
- Sponsor
- Namida Lab
HIV, Mental Health
NOLA GEM: Feasibility and Acceptability of an MHealth Intervention for Violence-affected PLWH
The objective of the proposed research is to conduct formative work to develop, pilot and refine a smartphone delivered intervention for violence affected people living with HIV utilizing a novel spatial-temporal methodology…
- Conditions
- HIV, Mental Health, Substance Use
- Trial name
- NCT05784714
- Testing
- NOLA GEM
- Where
- 4 sites in United States
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- Tulane University
Cancer Survivorship, Cancer
Finding My Way-UK: Promoting Positive Psychological Outcomes in People Living With and Beyond Curatively Treated Cancer
The goal of this pilot randomised trial is to evaluate whether an online psychosocial intervention (Finding My Way-UK) is feasible and acceptable for individuals living with and beyond curatively treated cancer.
- Conditions
- Cancer Survivorship, Cancer, Neoplasms
- Trial name
- FMW-UK (NCT07356726)
- Testing
- Finding My Way-UK, Treatment-As-Usual Control
- Where
- United Kingdom
- Volunteers
- 60 people
- Sponsor
- Edge Hill University
Substance Use Disorders
Home-based Continuing Care for Young Adults Leaving Residential Substance Abuse Treatment
The purpose of this project is to develop and test a Home-based Continuing Care intervention that will help parents support the recovery of their Young Adult (YA) child who is leaving residential substance abuse treatment.
- Trial name
- HCC (NCT02152033)
- Testing
- Home-based Continuing Care, Services as Usual
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- Treatment Research Institute
Placenta Praevia, Vaginismus
Transperineal Ultrasound to Assess the Progress of Labour
This is a prospective observational study of transperineal ultrasound between 24-42 weeks gestation and a prospective longitudinal observational study in all term (37-42 weeks) labouring women.
- Trial name
- NCT02430038
- Where
- United Kingdom
- Volunteers
- 584 people, healthy volunteers welcome
- Sponsor
- Imperial College London
PTSD
Evaluation of Psilocybin-assisted Psychotherapy (PaP) for the Treatment of Post-traumatic Stress Disorder (PTSD) in Military Veterans
Post-Traumatic Stress Disorder (PTSD) is a mental health condition that occurs as a result of a traumatic experience. Symptoms include feeling anxious, flashbacks, nightmares and difficulty sleeping.
- Trial name
- NCT05876481
- Testing
- Psilocybin
- Where
- United Kingdom
- Volunteers
- 8 people
- Sponsor
- Combat Stress
Upper Respiratory Infections
Warming Sensation Intensity and Acceptability of the Flavour, Local Tolerability of Paracetamol 500 mg + Phenylephrine 10mg + Guaifenesin 200 mg Syrup in Patients Suffering a Upper Respiratory Tract Infection (URTI)
This is an open label, in-use study to assess the warming sensation, acceptability and local tolerability of paracetamol 500 mg + phenylephrine 10mg + Guaifenesin 200 mg syrup, given as a single dose in subjects suffering from…
- Trial name
- NCT01576809
- Testing
- IFF flavor 316 282, Paracetamol , Phenylephrine, Guaifenesin
- Where
- Canada
- Volunteers
- 51 people
- Sponsor
- Novartis
Type 2 Diabetes Mellitus
Gastric Modulator (TANTALUS® System) Versus Insulin Treatment in Obese Type 2 Diabetic Patients - a Randomized Control Trial
This study aims to analyze the pre- and post-operative clinical, hormonal and biochemical changes in moderately obese type 2 diabetic patients who are sub-optimally controlled on at least 2 anti-diabetic agents.
- Trial name
- NCT00975533
- Testing
- Tantalus, Insulin
- Where
- China
- Volunteers
- 24 people
- Sponsor
- Chinese University of Hong Kong