Skip to content

Group-based Chronic Kidney Disease Care

Group-based Chronic Kidney Disease Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02467894
Enrollment
60
Registered
2015-06-10
Start date
2014-08-31
Completion date
2017-08-31
Last updated
2019-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Disease, Hypertension

Keywords

Adherence, Exercise

Brief summary

A two-group randomized clinical trial testing whether group-based care is feasible and will help improve blood pressure control in adult and adolescent patients with chronic kidney disease and hypertension.

Detailed description

This two-group RCT will enroll 100 subjects, adolescents over or equal to 12 years of age, and men and women over age of 21, with stage 3-4 and 5 CKD from various causes including diabetes and hypertension. Patients will be recruited from the Montefiore Medical Center Nephrology. The primary aim will be to assess feasibility of the intervention. Informed consent will be obtained on all subjects. All subjects with meet with one of the investigators who will verbally explain to them the purpose of the study and the alternatives. Blood and 24 hr urine test will be collected to assess for sodium, phosphorus, and serum creatinine. These tests will be used for experimental purposes only and will be collected at enrollment and 6 months visit. There will be two arms, an arm randomized to Group-based care attending monthly outpatient clinic visits as part of a group and the other to usual care who will see their provider once a month for 6 months.

Interventions

OTHERGroup-based Care

There will be self-care activities, blood pressure measurements and other vitals, including discussion of specific topics initiated by the participants.

Sponsors

Albert Einstein College of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adolescent Age ≥12 years old * Sufficient hearing, vision, and proficiency in English or Spanish to comprehend low- literacy printed educational materials and participate in group sessions (assessed by provider) * Adult: (¬\>21 years): Systolic blood pressure \>140 at two clinic visits in the past year or \>160 at one visit and Adolescent: (12-21 years) systolic blood pressure \>95 percentile (based on sex and age) at 2 clinic visits in the past year * For adults: Stage 3-5 CKD (eGFR\<60 ml/min/1.73m2) * For adolescents: evidence of kidney damage (albuminuria, congenital anomalies of the kidney or urinary tract) and hypertension * Prescription for anti-hypertensive medication (in adults) * Unwillingness to accept random assignment * Unwillingness to provide informed consent

Exclusion criteria

* Transplanted organ * Rapidly deteriorating kidney function with the expectation for initiation of dialysis in less than 6 months * Plans to relocate out of New York City in the next 6 months

Design outcomes

Primary

MeasureTime frameDescription
Blood pressure control6 monthsThe primary outcome will be blood pressure control (mean SBP \<140 mmHg) as measured by 24-hour ambulatory blood pressure monitor.

Other

MeasureTime frameDescription
Accelerometer6 monthsEvaluate effects of group-based care on physical activity
Medication Adherence6 monthsMeasured by the Morisky 8-item Medication Adherence scale.
Quality of Life6 monthsWe will collect quality of life measurements using the Peds QL in the adolescent group and the SF-36 in the adult sample. We want to evaluate whether group-based care may lead to improved or worse reported quality of life in participants.
Health Resources and Services Administration (HRSA)6 monthsEvaluate patient and provider satisfaction

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026