ClinicalTrials.Veeva

Menu

Effectiveness of 20m-MB in KTR Symptom Control

U

University of Malaya

Status

Completed

Conditions

Transplant;Failure,Kidney

Treatments

Other: 20-minute mindful breathing session

Study type

Interventional

Funder types

Other

Identifiers

NCT05809440
2020116-9206

Details and patient eligibility

About

To study the effectiveness of single session 20-minute mindful breathing in symptom control in kidney transplant recipients.

Full description

Patients undergoing kidney transplant follow ups in our center are screened based on recruitment criteria. Patients who fulfilled the incusion criteria are recruited. Intervention involves a 20-minute mindful breathing session with uniform script performed by trained personal, while control arm involves standard care without intervention.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult renal transplant patients aged 18 years and older
  • At least one symptom scoring ≥ 4/10 based on the Edmonton Symptom Assessment Scale (ESAS)

Exclusion criteria

  • Dialysis-dependent
  • Medically unstable
  • Having serious pre-existing mental health issues

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Intervention Group
Experimental group
Description:
A 20-minute mindful breathing session guided by a trained medical doctor. The session consisted of four 5-minute breathing exercises done consecutively. Participants were instructed to close their eyes and bring their attention to their breathing, and re-direct their attention back to their breathing once they were distracted.
Treatment:
Other: 20-minute mindful breathing session
Control Group
No Intervention group
Description:
No intervention was provided for control group.

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems