Clinical trials

23

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Using Smartphones to Improve Physical Activity Levels of Individuals With Spinal Cord Injury

The overarching goal of this research study is to evaluate a sensor-enabled, just-in-time adaptive intervention (JITAI) strategy to increase and sustain physical activity levels among individuals with spinal cord injury (SCI) in their communities. A primary objective of this study is to evaluate the integration of a JITAI with a web-based physical activity intervention program. We hypothesize that the integration of web-based physical activity intervention program with JITAI will result in significantly higher physical activity levels compared to the standard web-based physical activity intervention program alone. A secondary objective of this study is to extend existing algorithms that use commercial wearable technology to robustly detect physical activity behaviors to facilitate the delivery of tailored just-in-time actionable feedback and physical activity recommendations for individuals with SCI.

Participants needed: 196
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

18-75 years of age [+6]

any secondary complications that medically restrict their activity in any way su... [+1]

Status: Recruiting

Oropharyngeal Candidiasis (OPC) and S-ECC

The overall objective of this study is to investigate the association of early Candida infection (known as oral thrush or oropharyngeal candidiasis, OPC) in children during the first year of life with the onset and severity of severe early childhood caries (S-ECC).

Participants needed: 70
Trial details
Age: 9-15Biological sex: AllType: ObservationalSponsor: Temple UniversityUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Male or female individuals at the age of 9-15-month-old [+3]

Presence of a systemic medical condition (e.g. Down syndrome etc.) [+4]

Status: Not yet recruiting

Development and Test of a Communication Skills Training for Transplant Providers - Aims 2 & 3

The goal of this clinical trial is to understand the communication occurring between Black and Caucasian patients and their transplant providers during transplant evaluation consultations and assess relationships between these communicative elements and patient and provider factors, patient-reported outcomes and living donor transplant outcomes - living donor referrals, evaluations, and transplants. We will use these findings to inform the development of a communication skills training for transplant providers and test the impact of the training on providers' communication about live donor kidney transplants with Black and Caucasian patients and living donor transplant outcomes. The main questions it aims to answer are: * How does the use of the use of instrumental, relational and affective communication by patients and providers during the transplant consultation differ by patient and provider factors, patient-reported outcomes and patient ethnicity? * What elements of instrumental, relational and affective communication will be predictive of live donor kidney transplant (LDKT) process outcomes (LD inquiries and evaluations, and actual LDKTs)? Participants will be asked to complete brief surveys before and after the transplant consultation and to give permission for the consultation to be audiorecorded. This data will be used to develop a training to educate providers on the key communication factors predictive of LDKT process outcomes specific to Black and Caucasian patients, and provide guidance on their application during patient consultations. Researchers will then compare communication and patient-reported and LDKT process outcomes between trained and untrained providers to see whether the training has any effect on living donor inquiries and evaluations, and actual LDKTs.

Participants needed: 70
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Jun 12, 2026Locations: 2
Eligibility criteria

(1) appear for a kidney transplant evaluation at Cooperman Barnabas Medical Cent... [+6]

(1) are non-verbal or otherwise unable to converse with providers [+2]

Status: Not yet recruiting

Testing a Mobile Health Application to Improve HIV Prevention and Substance Use Treatment Among Women Involved in the Carceral System

Women involved in the carceral system (WICS) are at higher risk for both HIV and substance use than the general public. WICS are also more likely to engage in behaviors both before and after release that put them at risk for HIV and for overdose, due to opioid use. Despite these risk factors, WICS are less likely to be aware of, use, or adhere to pre-exposure prophylaxis (PrEP) and have less access to medications for opioid use disorder (MOUD). The primary goal of the proposed research is to pilot test a systematically developed PrEP and MOUD uptake intervention for WICS using contextually relevant messages developed through novel formative research methods and embedded in a web-based application in a rigorous research design. The investigators will then test this approach (called PA-LINKS) in a pilot randomized trial with women who have recently been incarcerated in Philadelphia in partnership with Philadelphia FIGHT, a federally qualified health center, for promise of efficacy, and to assess feasibility and acceptability.

Participants needed: 74
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Temple UniversityUpdated: May 13, 2026Locations: 1
Eligibility criteria

18 of years of age or older [+7]

Under 18 years old [+8]

Status: Recruiting

RemI for Post-Bariatric Surgery Weight Regain

The goal of this clinical trial is to test the effectiveness of remotely-delivered interventions (utilizing acceptance-based behavioral treatment skills (ABTi)) amongst bariatric surgery populations who are experiencing weight regain postoperatively (\> 5% from their lowest postoperative weight and after postoperative Month 6). Investigators aim to evaluate ABTi's efficacy for reversing weight regain and its effect on targeted weight control behaviors and weight-related comorbidities by comparing participants randomly assigned ABTi (n = 100) to those assigned to a Control group that also receives brief phone calls but that focus on reiterating instruction on the dietary and behavioral changes required of surgery and initially taught preoperatively (C, n = 100). The main research aims are: 1. To compare changes in body weight over 12 months in 200 bariatric patients who have regained \> 5% of their weight and are randomly assigned to ABTi or Control. 2. To compare changes in eating behaviors (i.e., caloric intake, frequency of maladaptive eating behaviors), physical activity, and weight-related comorbidities (i.e., biomarkers of diabetes, hypertension) over 12 months in the two groups. 3. Exploratory - To test ABTi's theoretical mechanisms of action, including a) effects of theory-based active ingredients (i.e., acceptance, defusion, values clarity, mindfulness) on weight outcomes and b) changes in impact of internal states (i.e., hunger, cravings) on eating behavior.

Participants needed: 200
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Apr 3, 2026Locations: 2
Eligibility criteria

Men and women [+6]

Long-term treatment with oral steroids [+9]

Status: Not yet recruiting

Comparing the Impact of Peer Support vs. Staff-Delivered Transportation Interventions for Young Adults With Intellectual and Developmental Disabilities.

This clinical trial will look at whether young adults with intellectual and developmental disabilities (YA-IDD) have better outcomes when a travel training intervention called Ready to Ride (R2R) is taught by a specially trained Peer Supporter (PS) who shares the lived experience of having an IDD than YA-IDD who are taught Ready to Ride by staff at their community services organization. The aspects of life being looked at are loneliness, satisfaction with social activities, travel skills, service use and access, employment, and health related quality of life. The researchers think the following things will happen. 1. YA-IDD who learn from a Peer Supporter will report significantly higher satisfaction with social activities, increased social connectedness and significantly less loneliness compared to YA who are taught organization staff. 2. Both groups will learn the same amount of travel skills. 3. YA-IDD who learn from a Peer Supporter will show larger increases in access to community-based services, transportation use, employment and health related services after 4 months than the YA taught by organizational staff.

Participants needed: 325
Trial details
Age: 18-27Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Apr 1, 2026Locations: 3
Eligibility criteria

Between the ages of 18 to 27 years old during the start of the study [+4]

Independently uses public transportation >4 times/month. [+2]

Status: Recruiting

Optimizing the Prehospital Use of Stroke Systems of Care-Reacting to Changing Paradigms-Implementation (OPUS-i)

This interventional trial will compare a novel prehospital stroke transport algorithm (OPUS-i) to a traditional prehospital stroke transport algorithm to improve outcomes in rural stroke patients by determining the effect of implementing a data-driven prehospital stroke algorithm on time to and endovascular therapy. The study consists of a multicenter cohort and will last 24 months but individual subject study duration is 90 days.

Participants needed: 360
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Mar 12, 2026Locations: 2
Eligibility criteria

Clinical impression of stroke/TIA by EMS clinicians

Age < 18 years [+1]

Status: Recruiting

Non-invasive Vagus Nerve Stimulation (nVNS) and Cognition in Young Adult Vapers - A Pilot Study

The purpose of this study is to assess the effects of non-invasive vagus nerve stimulation (nNVS) on cognitive functioning in the users of e-cigarettes or vaping products. The investigators will use a digital wellness companion product (TRUVAGA™ device) that provides mild transcutaneous nVNS. The participants will be randomized to receive either a 2-min nNVS stimulation or control stimulation in the neck region followed by completion of three cognitive tests of attention and executive function.

Participants needed: 100
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Mar 6, 2026Locations: 1
Eligibility criteria

Healthy young adults [+2]

Have any rash, infection, swelling, cut, soreness, drug patch, surgical scar on... [+18]

Status: Recruiting

Brief Behavioral Sleep Intervention for Obesity Prevention in Primary Care

The goal of this study is to compare two different approaches to help families with children 6-11 years enhance nighttime sleep: 1) working one-on-one with a nurse to learn effective behavioral strategies to try to improve children's sleep or 2) receiving education on a good night's sleep and its benefits. Participating families will meet with a nurse 6 times or receive 6 educational handouts. Participating families will also complete three assessments (start of the study, 2 months and 6 months) during which study questionnaires will be completed, participating children will wear devices that assess sleep and physical activity, participating families will report on what the child ate on two separate days and will be measured for height and weight.

Participants needed: 50
Trial details
Age: 6-11Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Feb 12, 2026Locations: 1
Eligibility criteria

Patient at Temple Pediatrics [+6]

Diagnosed sleep disorder [+2]

Status: Recruiting

Need to be Needed (N2BN) Intervention

The proposed study is a randomized, controlled trial (RCT) that will examine the effectiveness of an intervention designed to reduce social isolation and loneliness of adults with serious mental illness (SMI). The intervention will focus on improving their sense of mattering by using acts of kindness and experiencing gratitude through volunteering. 120 participants will be randomly assigned to the intervention group or the attention control group. Over the course of the 6-month intervention, participants in the intervention arm, will receive weekly support from the interventionist. The interventionist and the participant will collaboratively set goals and develop an initial intervention plan, which is informed by the participants interests, values and goals. The attention control group will receive non-directive listening support through research assistants. Data collection for all participants will occur at baseline, at the mid-point of the intervention at 3 months, and at the end of the 6-month intervention. Participants will be asked questions about quality of experience, social context and satisfaction, mattering components, kindness, gratitude, and loneliness. We will gather data on demographic background, life transitions, social network characteristics, internalized stigma, neighborhood climate, depression, and trait measures of mattering and loneliness during intake and exit interviews. Additionally, participants of the intervention arm will be asked to provide feedback about the intervention.

Participants needed: 120
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Jan 21, 2026Locations: 1
Eligibility criteria

A research diagnosis of Major Depression, Bipolar I, II, or Schizophrenia Spectr... [+4]

Having a legal guardian [+2]

Status: Recruiting

Photo-experiencing and Reflective Listening (PEARL) to Promote Healing Engagement for Survivors of Violence

The goal of this clinical trial is to learn if a photo-elicitation intervention called PEARL (Photo-experiencing and Reflective Listening) can promote healing engagement in survivors of interpersonal violence. It will also learn about the feasibility and acceptability of PEARL. The main questions it aims to answer are: Does PEARL reduce barriers to help-seeking for trauma? Does PEARL improve trauma coping self-efficacy? Does PEARL change post-trauma cognitions and readiness for recovery? Is PEARL feasible and acceptable to survivors of interpersonal violence? Researchers will compare people who receive PEARL immediately to people on a waitlist (who receive PEARL three months later) to see if PEARL improves healing engagement and help-seeking behaviors. Participants will: * Complete baseline surveys about their trauma history, mental health, healing, and help-seeking behaviors * Be randomly assigned to receive PEARL immediately or after a 3-month wait * Receive a photography-focusing prompt and create photos over two weeks (those in the immediate group or after the waiting period) * Participate in a reflective listening interview about their photos * Complete follow-up surveys immediately after the intervention and one month later * Participate in a one-month follow-up interview about their experience

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

Age 18 years or older [+3]

Under 18 years of age [+4]

Status: Recruiting

Taking Action for College Students

The goal of this research is to investigate whether a peer-delivered illness self-management program called Taking Action can help college students with serious mental illnesses. Participants will be randomly assigned to either the experimental condition (Taking Action) or the control condition (information only). Participants in the experimental condition will attend five 2.5-hour Taking Action sessions. Participants will complete three interviews (baseline, post-intervention, and follow-up) to assess how well the program works, is liked, and benefits students clinically and academically. The investigators seek to test the following hypotheses: Compared to controls, students who do the Taking Action program will report greater improvements in mental health self-management attitudes, skills, and behaviors and will report greater improvements in mental health symptoms and recovery, and better academic outcomes.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Dec 29, 2025Locations: 1
Eligibility criteria

Currently enrolled in a 2- or 4-year postsecondary educational institution in th... [+5]

Expected to graduate or complete their program within 2 semesters [+1]

Status: Recruiting

The Path to Optimal Black Maternal Heart Health: Comparing Two CVD Risk Reduction Interventions (Change of HEART)

The overarching goal of our proposal is to reduce disparities in perinatal cardiovascular disease risk factors among Black women utilizing a community-driven, social ecological framework.

Participants needed: 432
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Temple UniversityUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

age ≥18 years [+4]

Status: Recruiting

Nurturing Needs Study: Parenting Food Motivated Children

High food motivation among children is trait-like and increases risks of unhealthy dietary intake and obesity. Scientific knowledge of how parenting can best support healthy eating habits and growth among children who are predisposed to overeating is surprisingly limited. This investigation will identify supportive food parenting approaches for obesity prevention that address the needs of highly food motivated children.

Participants needed: 416
Trial details
Age: 4-5Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Nov 5, 2025Locations: 2
Eligibility criteria

Child ages 4 or 5 years at baseline; [+3]

Parent/primary caregiver <18 years of age; [+3]

Status: Recruiting

InformationSeekingMesolimbicEngagementStudy2

Participants will complete a treasure task during neuroimaging where they have to learn which keys open a treasure chest, and then they are tested on the contents of the treasure chest.

Participants needed: 80
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Sep 5, 2025Locations: 1
Eligibility criteria

20/40 far acuity (either corrected or uncorrected) [+1]

History of head injury [+6]

Status: Recruiting

Prospective Validation of the Novel PVD-B65 Risk Score in Patients With Chronic Lung Disease and Pulmonary Hypertension

Prospective observational study to determine if the PVD-B65 risk score for one-year mortality in patients with chronic lung disease and pulmonary hypertension (CLD-PH) can accurately risk stratify these patients and successfully predict one-year mortality from time of pulmonary hypertension diagnosis. PVD-B65 risk score was developed in a retrospective cohort of patients with CLD-PH, utilizing the presence of pulmonary fibrosis without emphysema, pulmonary vascular resistance (PVR) \> 5 woods units (WU), 6-minute walk distance (6MWD) \< 150 meters, B-natriuretic type peptide (BNP) \> 200 pg/mL or N-terminal pro-natriuretic type peptide (NT-proBNP) \> 300 pg/dL, and age \> 65 years as the score components.

Participants needed: 100
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: Temple UniversityUpdated: Sep 3, 2025Locations: 1
Eligibility criteria

Eligibility criteria [+5]

Exclusion criteria [+3]

Status: Not yet recruiting

A Trauma-Informed Intervention for the Newly HIV-Diagnosed

The current approach to HIV prevention emphasizes: (1) achieving viral suppression among HIV+ people in order to reduce HIV transmissibility, particularly for disproportionately affected groups such as Black sexual minority men (BSMM), by increasing retention in HIV care, and (2) addressing comorbidities and complications, which include mental health concerns such as trauma symptomology and severe acute stress reactivity. Despite the disproportionate impact of both HIV and traumatic stress on BSMM and the adverse effects of stress on engagement in HIV care, BSMM remain grossly underserved with respect to mental health. To address these gaps, the proposed study will develop an intervention that will: (1) provide a brief, resilience-oriented, trauma-informed intervention that combines online sessions and highly tailored text-messaging to reduce participant burden and motivate clients between sessions, (2) provide preliminary treatment for HIV+ BSMM's unaddressed mental health needs, and (3) be embedded early in the HIV continuum of care immediately after diagnosis to facilitate linkage to and retention in HIV care.

Participants needed: 80
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: Temple UniversityUpdated: Jul 8, 2025
Eligibility criteria

Diagnosed with HIV within the past 3 months [+5]

Demonstrating cognitive impairment or acute psychosis [+1]

Status: Recruiting

Temple Health Chest Initiative (THCI 2.0)

Chronic obstructive pulmonary disease is highly prevalent globally, with considerable morbidity and mortality associated. In the US, it is the 4th leading cause of death, as well as contributing to significant costs on healthcare utilization including hospitalization. Population-based screening for COPD has not been recommended by the US Preventative Services Task Force (USPSTF). However, LDCT screening for lung cancer in patients aged 50- 80 with ≥ 20 pack year smoking has been shown to improve survival. COPD is highly prevalent within LCS programs, with estimated rates of obstructive lung function of up to 59% and evidence of emphysema on CT scan in around 70%.

Participants needed: 1,000
Trial details
Age: 50-80Biological sex: AllType: ObservationalSponsor: Temple UniversityUpdated: Apr 18, 2025Locations: 1
Eligibility criteria

50 to 80 years old [+1]

Under 50; over 80 years old [+1]

Status: Recruiting

Food for Thought: Executive Functioning Around Eating Among Children

Scientific knowledge of the cognitive-developmental processes that serve to support children's appetite self-regulation are surprisingly limited. This investigation will provide new scientific directions for obesity prevention by elucidating cognitive-developmental influences on young children's ability to make healthy food choices and eat in moderation.

Participants needed: 125
Trial details
Age: 4-6Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Apr 10, 2025Locations: 1
Eligibility criteria

Child ages 4 to 6 years of age [+2]

Caregiver <18 years of age [+3]

Status: Not yet recruiting

Machine Learning to Reduce Hypertension Treatment Clinical Inertia

Among individuals with an uncontrolled BP at the current visit, the objective of this study is to compare clinical management of hypertension with and without information from a machine learning algorithm on whether a patient will have uncontrolled blood pressure at their next follow up visit through a case-vignette study.

Participants needed: 50
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Apr 10, 2025
Eligibility criteria

Not listed

Status: Recruiting

myAirvo 3 (High Flow Nasal Therapy; HFNT) for COPD Patients in the Home

Parallel-group, prospective, randomized, controlled phase III trial of home High flow Nasal Therapy (HFNT) via myAirvo 3 plus usual COPD medical care vs. usual COPD medical care, for at least 1 year and up to two years in 642 GOLD Grade D, Stages II-IV patients with moderate to very severe COPD at risk for moderate and severe exacerbations with a prior history of severe exacerbation requiring hospitalization within the past 6 weeks.

Participants needed: 642
Trial details
Age: 30+Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Feb 6, 2025Locations: 27
Eligibility criteria

Provision of signed and dated informed consent form [+20]

Current self-reported chronic use of positive airway pressure (PAP) therapy; con... [+9]

Status: Recruiting

Peer Facilitated Waitlist Controlled Transportation Study

The goal of this clinical trial is to test the effectiveness of a peer-facilitated travel intervention in adults with serious mental illnesses. This project aims to address the following hypotheses: 1. Individuals with SMI receiving either of the two peer-mediated travel training transportation interventions will experience an increase in transportation self-efficacy and transportation skills. 2. Participants in the intervention arms will increase their transport utilization, participate in significantly more activities in the community, and make significantly more trips in the community. 3. Individuals with SMI receiving peer-mediated travel training interventions will retain post-test levels of community participation and self-efficacy 2 months after intervention. Participants will be assigned to an 8-week travel-training intervention either using a bike-share program or public transportation. All participants will complete three data-collection research interviews.

Participants needed: 180
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Nov 1, 2024Locations: 1
Eligibility criteria

are between the ages of 18 and 65 [+5]

score less than 8 on a travel skills assessment [+5]

Status: Not yet recruiting

Community Navigators

The Temple University Collaborative on Community Inclusion (TU Collaborative) is testing a community navigation intervention study based upon effective health navigation models by conducting a randomized controlled trial of the intervention to establish feasibility, efficacy, and outcomes among adults with serious mental illness (SMI).

Participants needed: 96
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Temple UniversityUpdated: Sep 19, 2024
Eligibility criteria

meet the criteria for an SMI diagnosis of schizophrenia, schizoaffective, bipola... [+4]

inability to provide consent (legal guardian) [+1]