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Intradıalytıc Weıght Control In Hemodıalysıs Patıents (DialysisSuit)

B

Balikesir University

Status

Completed

Conditions

Fluid Overload

Treatments

Behavioral: control group
Behavioral: suit group
Behavioral: training group

Study type

Interventional

Funder types

Other

Identifiers

NCT07030361
BalikesirUniversity HealtScien
222S306 (Other Grant/Funding Number)

Details and patient eligibility

About

The aim of this observational study is to determine the effect of a dialysis gown designed according to the empowerment model on changes in weight control behaviors among gown group patients during the intradialytic period. The main question it seeks to answer is:

• Is the dialysis gown effective in helping gown group patients control their fluid intake during the intradialytic period?

Full description

In this study, researchers designed a study to compare whether the behavior of controlling excessive fluid intake during the intradialytic period was better in the group of patients wearing dialysis garments designed according to the empowerment model than in the education and control groups. For this randomized controlled study, patients were divided into three groups. The patients were named the garment group, the education group, and the control group. In the study design, patients underwent garment application and education application. In the garment application, the amount of excess fluid removed by ultrafiltration during that dialysis session was placed in the pockets of the serum dialysis garment, and patients were asked to walk in a 10-meter walking test area. In the education application, a video-based education program designed to teach fluid compliance behavior was implemented. Patients were asked to watch this video education program for an average of half an hour at the beginning of each session.

Patients in the garment group were dressed in dialysis garments and shown the educational video. Patients in the education group were only shown the fluid compliance video. No intervention specific to the study was performed on patients in the control group. All patients continued to receive the normal follow-up and care protocol required for hemodialysis treatment.

Enrollment

66 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Turkish-speaking
  • Turkish-understanding
  • Older than 18 years of age
  • Without communication barriers such as visual and hearing impairment
  • Non-hypotensive and non-anemic patients
  • With an intradialytic weight of 2-5 liters
  • Receiving hemodialysis treatment for more than three months and outpatients

Exclusion criteria

  • Patients who had previously received fluid restriction compliance training
  • Who refused to participate in the study
  • Who had undergone surgery within the last six weeks

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

66 participants in 3 patient groups, including a placebo group

suits group
Active Comparator group
Description:
Dialysis suit group was dressed in dialysis suit and given fluid control training
Treatment:
Behavioral: suit group
2 training group
Placebo Comparator group
Description:
Fluid control training was given to the traininig group
Treatment:
Behavioral: training group
control group
Other group
Description:
Control group received no intervention, clinical care
Treatment:
Behavioral: control group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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