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ACMMPDFBApplication of Contract Management Mode in Maintaining Body Fluid Balance of Peritoneal Dialysis Patients

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What is being tested

Contract management

Behavioral
Who is being recruted

From 18 to 65 Years
+10 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Services Research Study

Interventional
Study Start: June 2016
See protocol details

Summary

Principal SponsorThe Second Affiliated Hospital of Harbin Medical University
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: June 1, 2016

Actual date on which the first participant was enrolled.

Contract management is a new management mode, it stipulate and constraint various relationship by various duties, institutions and regulations. To help patients achieve fluid balance through contract management, that is: 1. edema, congestive heart failure and other similar symptoms begin to reduce to disappear; 2. Blood pressure control in normal range, that is 90-140/60-90mmHg, or the target value prescribed by the doctors; 3. Fluid intake and output keep in balance; 4. No imbalance symptoms turn out, such as edema, congestive heart failure, etc. In addition to help keeping the fluid balance through contract balance, but also: 1. Improve compliance; 2. Improve the patients' cognition of fluid balance; 3. Improve the ability of self-management of fluid balance.

Official TitleApplication of Contract Management Mode in Maintaining Body Fluid Balance of Peritoneal Dialysis Patients
NCT02782234
Principal SponsorThe Second Affiliated Hospital of Harbin Medical University
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

72 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Services Research Study

These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

4 inclusion criteria required to participate
Older or equal to 18 years, younger or equal to 65 years, CAPD duration over 6 months

Edema or congestive heart failure happen

Patients with poor control of blood pressure, that is less than 90/60mmHg,or over 140/90mmHg, or the Bp does not meet the value given by doctors

Patients with fluid imbalance of intake and output.

6 exclusion criteria prevent from participating
Younger than 18, or older than 65, or CAPD period less than 6 months

The primary disease is high blood pressure, or edema due to low protein

Patients that lost control of daily life

Malignant tumor or pregnancy

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
In accordance with the contract content, researchers and participants should manage and maintain the liquid balance of the participants. Signed doctors and nurses should undergo the follow-up phone or family visit on time, instruct them proper healthy training, and provided necessary information data. By telephone, SMS, wechat, remind and urge the participants to take the lifestyle and behavior regulate in the contract. Participants should supervise and manage the fluid unbalance (Edema, hypertension, heart failure, and fluid imbalance of intake and output etc.), and feedback the Management and supervision to researchers according to contract.

Study Objectives

Primary Objectives

Study Centers

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