clinical-trials

Clinical Trials Digest (July 22, 2026): 7 recruiting studies, many with at-home options

A plain-language roundup of 7 recruiting clinical studies (with links) that may be remote-friendly. Each listing includes what you might do, estimated visits, time, and rough compensation-for-time estimates based on public details.

Here are 7 recruiting clinical research studies, summarized in simple terms. Many include at-home (remote) parts like apps, surveys, phone/video check-ins, or mailed kits, but some still need in-person visits. Always read the official study page and ask the study team questions.

Compensation ranges below are rough estimates for time burden only, not sponsor-provided offers.

Informational only, not medical advice.

1) Mobile app + coaching to increase activity (women, DC area) — NCT03288207

NCT ID: NCT03288207

Source: clinicaltrials.gov study page

This study is testing whether a mobile app and remote coaching (sometimes tailored to your neighborhood) can help people move more. It focuses on African American women who are overweight or have obesity and live in specific areas near Washington, DC. Some parts may be remote, but visits at the NIH Clinical Center in Bethesda, Maryland may be needed, and MRI may be optional.

Who may be able to join (high level): African American women ages 21–75, overweight/obese, living in DC Wards 5/7/8 or nearby Prince George’s County, with a compatible smartphone.

What you may need to do

  • Answer surveys in an app (about health, activity, and related topics)
  • Wear a wrist device that tracks steps and sleep
  • Use the study app and receive messages/coaching
  • Do blood tests at certain visits
  • Possibly use at-home wireless devices (like a scale or other monitors) and upload readings
  • Optional imaging like MRI (if eligible)

Estimated visits needed: About 4–12 visits (estimate, not guaranteed; based on public details)

Estimated time commitment: About 8–53 total hours (estimate, not guaranteed; based on public details)

Estimated compensation for time: About $275–$4500 total (estimate, not guaranteed; based on public details)

Contacts (from public listing):

See if you qualify

2) Sharing health + genetic info to help build better data tools — NCT05657405

NCT ID: NCT05657405

Source: clinicaltrials.gov study page

This observational study collects medical and genetic-related information from people with known or suspected genetic conditions, or from family members of someone with a suspected genetic condition. The goal is to help researchers develop better computer tools (like advanced analytics) to understand genetic conditions. Some people may be able to do parts by telehealth, but some testing may happen at the NIH Clinical Center in Bethesda, Maryland.

Who may be able to join (high level): People of any age with a known/suspected genetic condition, or a relative of someone with a known/suspected genetic condition.

What you may need to do

  • Share medical history information
  • Provide samples like blood or saliva/cheek swabs
  • Possibly do imaging (like X-rays or other scans) depending on your situation
  • Possibly do heart tests (examples listed include tests done while lying still)
  • Possibly provide photos, video, or audio recordings (for research documentation)
  • Some follow-ups may be by phone/video

Estimated visits needed: About 2–6 visits (estimate, not guaranteed; based on public details)

Estimated time commitment: About 7–28 total hours (estimate, not guaranteed; based on public details)

Estimated compensation for time: About $325–$3350 total (estimate, not guaranteed; based on public details)

Contacts (from public listing):

See if you qualify

3) At-home joint health supplement study (knee osteoarthritis symptoms) — NCT07493239

NCT ID: NCT07493239

Source: clinicaltrials.gov study page

This decentralized (mostly at-home) study compares two doses of a dietary supplement called MyCondro™ in adults with self-reported mobility issues linked to knee osteoarthritis. The main measure is how participants report their pain, stiffness, and function over about 12 weeks, using surveys in an app.

Who may be able to join (high level): Adults age 45+, BMI 18–35, with a known diagnosis of knee osteoarthritis and ongoing mobility issues, living in the U.S., with a smartphone and internet.

What you may need to do

  • Download and use the Chloe app (People Science) for surveys
  • Take the study product daily (either 300 mg or 600 mg; assigned randomly)
  • Complete regular questionnaires about symptoms and daily life
  • Use wearable tracking (to measure activity)
  • Do at-home blood sample collection (kit-based) for some measures
  • Join phone/video check-ins if scheduled

Estimated visits needed: About 4–12 visits/check-ins (estimate, not guaranteed; based on public details)

Estimated time commitment: About 8–53 total hours (estimate, not guaranteed; based on public details)

Estimated compensation for time: About $275–$4500 total (estimate, not guaranteed; based on public details)

Contacts (from public listing):

See if you qualify

4) Fully remote physical activity program for older Hispanic/Latino(a) adults — NCT06362824

NCT ID: NCT06362824

Source: clinicaltrials.gov study page

This study tests a culturally adapted, fully remote program (De Pie y a Movernos) meant to help older Hispanic/Latino(a) adults become more physically active. Participants are randomized to either the De Pie program or a comparison program about general brain health topics. The program period is about 12 weeks.

Who may be able to join (high level): Hispanic/Latino(a) adults ages 55–89 without dementia, with a smartphone, able to read Spanish or English, and able to walk one block unassisted. Recruitment is tied to Southern California and Kaiser Permanente Washington.

What you may need to do

  • Join phone calls with staff during weekday business hours
  • Wear an activity monitor (ActiGraph) for up to 2 weeks, twice
  • Complete questionnaires by web link, paper, or phone
  • Take part in the assigned program (intervention or comparison)

Estimated visits needed: About 4–12 visits/check-ins (estimate, not guaranteed; based on public details)

Estimated time commitment: About 7–38 total hours (estimate, not guaranteed; based on public details)

Estimated compensation for time: About $250–$3225 total (estimate, not guaranteed; based on public details)

Contacts (from public listing):

See if you qualify

5) Environment + activities (including virtual reality) and drinking behavior — NCT06860607

NCT ID: NCT06860607

Source: clinicaltrials.gov study page

This pilot study looks at how different kinds of activities and environments might affect alcohol use and related feelings in people with alcohol use disorder (AUD). It includes in-person sessions in Baltimore, Maryland, plus app-based questions during daily life. The public summary says that during some lab visits, participants may be served one alcoholic drink and asked questions afterward.

Who may be able to join (high level): Adults 21+ with AUD who have a smartphone and can complete English-language assessments, and who meet study-specific safety and drinking-history criteria.

What you may need to do

  • Attend in-person sessions (some described as 3 hours long)
  • Use a phone app (MetricWire) to answer questions multiple times per day
  • Do screening/baseline tests (may include physical exam, blood/urine tests, breath alcohol test)
  • Take part in activity sessions (may include VR and other activities) and video-watching sessions
  • Do “bar-like room” assessments about cravings/urges; public summary notes one alcoholic drink may be provided on certain visits

Estimated visits needed: About 4–12 visits (public summary mentions up to 10) (estimate, not guaranteed; based on public details)

Estimated time commitment: About 11–62 total hours (estimate, not guaranteed; based on public details)

Estimated compensation for time: About $500–$7450 total (estimate, not guaranteed; based on public details)

Contacts (from public listing):

See if you qualify

6) Metformin before pregnancy to lower the chance of severe nausea/vomiting returning — NCT07129473

NCT ID: NCT07129473

Source: clinicaltrials.gov study page

This study is testing whether metformin extended-release (metformin-XR), taken before pregnancy and in early pregnancy, may reduce the risk and severity of hyperemesis gravidarum (HG) in people who had HG in a past pregnancy and are trying to conceive. There is a treatment group (metformin-XR plus surveys) and a survey-only comparison group (no study drug). Some visits and blood draws are listed for the treatment group.

Who may be able to join (high level): Females ages 18–49 who had HG in a prior pregnancy (public listing notes IV fluid treatment) and are trying to conceive; additional criteria apply. The public listing notes treatment-arm location limits (California/Alabama).

What you may need to do

  • Complete online questionnaires before pregnancy, during early pregnancy, and after birth (if pregnancy occurs)
  • If in the treatment group: take daily metformin-XR as instructed (dose increases over time)
  • If in the treatment group: attend brief study visits and do blood draws at certain timepoints
  • Track weight (public listing mentions owning a scale or being willing to get one)
  • Follow study timing rules about when to try to conceive (treatment arm specifics apply)

Estimated visits needed: About 4–12 visits (estimate, not guaranteed; based on public details)

Estimated time commitment: About 12–82 total hours (estimate, not guaranteed; based on public details)

Estimated compensation for time: About $550–$9850 total (estimate, not guaranteed; based on public details)

Contacts (from public listing):

See if you qualify

7) Two ways to help older adults (and caregivers) after leaving the hospital — NCT07661355

NCT ID: NCT07661355

Source: clinicaltrials.gov study page

This study compares two hospital-to-home transition support programs for older adults and their family caregivers. One program focuses on the patient, and the other adds extra family caregiver support. The goal is to see which approach helps people spend more days out of the hospital after discharge. The public listing says the study may use telephone/video calls and other technology depending on what families prefer.

Who may be able to join (high level): Patients age 65+ being discharged home from certain hospitals, plus an adult family caregiver willing to participate; English and Spanish speakers are included. Many clinical and discharge criteria apply.

What you may need to do

  • Take part as a patient-caregiver pair (a “dyad”)
  • Answer questions about health and daily functioning after discharge
  • Join phone or video calls with the study team
  • Caregivers may receive training/support as part of one program

Estimated visits needed: About 4–12 visits/check-ins (estimate, not guaranteed; based on public details)

Estimated time commitment: About 10–51 total hours (estimate, not guaranteed; based on public details)

Estimated compensation for time: About $450–$6125 total (estimate, not guaranteed; based on public details)

Contacts (from public listing):

See if you qualify

Reminder: Details can change, and “estimated” numbers above are non-guaranteed and based on public details. Always confirm the latest information (including payments, visit count, and what is remote vs. in-person) with the study team.

Informational only, not medical advice.

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