Effects of TRF on Obese Patients With CKD Stage 3-4

Sponsor
Guangdong Provincial Hospital of Traditional Chinese Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT05037747
Collaborator
(none)
28
1
2
10.6
2.6

Study Details

Study Description

Brief Summary

Obesity is associated with glomerular hyperfiltration leading to renal impairment and is a risk factor for the progression of kidney disease.Weight loss can reduce proteinuria and improve eGFR.Intermittent fasting is safe and effective, and in addition to improving body shape and weight in obese patients, it can also improve glucolipid metabolism, reduce proteinuria, improve kidney function and delay the progression of kidney disease.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Time-restricted feeding(TRF)
N/A

Detailed Description

KDOQI clinical practice guideline for nutrition in chronic kidney disease (CKD) uses a low-protein diet to reduce renal impairment and delay progression. The current research hotspot is dietary intervention. Time-restricted feeding was used to intervene in the progression of CKD. It restrict the time of eating but not the eaten calories, which have a higher compliance and safety. Studies have shown that intermittent fasting in obese patients with CKD is not only reduce body weight, but also improves glycolipid metabolism, reduces proteinuria and delays the progression of kidney disease. Intermittent fasting is currently a scientific research hotspot, and there are few international studies on the implementation of intermittent fasting to delay the deterioration of renal function in obese CKD patients, and lack of data on Chinese patients, which has great research potential. Based on the above background, this study was conducted as an pilot clinical trial to explore the effects of intermittent fasting on obese patients with CKD and to observe its effectiveness, safety and compliance.

Study Design

Study Type:
Interventional
Actual Enrollment :
28 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
It was non-randomized trial study design, two parallel groups were assigned to time-restricted feeding(TRF) and control group and to do the intervention for 12 weeks.It was non-randomized trial study design, two parallel groups were assigned to time-restricted feeding(TRF) and control group and to do the intervention for 12 weeks.
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Effects of Time-restricted Feeding on Obese Patients With Chronic Kidney Disease Stage 3-4: a Pilot Study
Actual Study Start Date :
Aug 12, 2021
Actual Primary Completion Date :
Mar 30, 2022
Actual Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Time-restricted feeding(TRF)

The TRF group was asked to restrict the eating window to 8 hours a day, during waking hours and also continue a low-protein diet.

Behavioral: Time-restricted feeding(TRF)
The TRF group was asked to restrict the eating window to 8 hours a day, during waking hours and also continue a low-protein diet.

No Intervention: Control

The control group was asked to continue their usual low-protein diet eating schedule and pattern.

Outcome Measures

Primary Outcome Measures

  1. Change in eGFR (ml/min/1.73m2) [12 weeks]

    eGFR at final visit - eGFR at initial visit

Secondary Outcome Measures

  1. Changes in body weight (Kilograms) [12 weeks]

    body weight at final visit - body weight at initial visit

  2. Changes in waist circumference (cm) [12 weeks]

    waist circumference at final visit - waist circumference at initial visit

  3. Change in body mass index (kg/m2) [12 weeks]

    body mass index at final visit - body mass index at initial visit

  4. Changes in serum total cholesterol levels (mmol/L) [12 weeks]

    serum total cholesterol levels at final visit - serum total cholesterol levels at initial visit

  5. Changes in serum low density lipoprotein cholesterol levels (mmol/L) [12 weeks]

    serum low density lipoprotein cholesterol levels at final visit - serum low density lipoprotein cholesterol levels at initial visit

  6. Changes in serum triglyceride levels (mmol/L) [12 weeks]

    serum triglyceride levels at final visit - serum triglyceride levels at initial visit

  7. Changes in serum high density lipoprotein cholesterol levels (mmol/L) [12 weeks]

    serum high density lipoprotein cholesterol levels at final visit - serum high density lipoprotein cholesterol levels at initial visit

  8. Changes in serum albumin (g/L) [12 weeks]

    serum albumin at final visit - serum albumin at initial visit

  9. Changes in total serum protein (g/L) [12 weeks]

    total serum protein at final visit - total serum protein at initial visit

  10. Changes in fat free mass (kg) [12 weeks]

    fat free mass at final visit - fat free mass at initial visit

  11. Changes in body fat mass (kg) [12 weeks]

    body fat mass at final visit - body fat mass at initial visit

  12. Changes in percent body fat (%) [12 weeks]

    percent body fat at final visit - percent body fat at initial visit

  13. Changes in waist-hip ratio [12 weeks]

    waist-hip ratio at final visit - waist-hip ratio at initial visit

  14. Changes in soft lean mass (kg) [12 weeks]

    soft lean mass at final visit - soft lean mass at initial visit

  15. Changes in visceral fat area (cm2) [12 weeks]

    visceral fat area at final visit - visceral fat area at initial visit

  16. Changes in arm circumference (cm) [12 weeks]

    arm circumference at final visit - arm circumference at initial visit

  17. Changes in triceps skin fold thickness (cm) [12 weeks]

    triceps skin fold thickness at final visit - triceps skin fold thickness at initial visit

  18. Changes in grip strength (kg) [12 weeks]

    grip strength at final visit - grip strength at initial visit

  19. Changes in fasting blood glucose (mmol/L) [12 weeks]

    fasting blood glucose at final visit - fasting blood glucose at initial visit

  20. Changes in serum creatinine (umol/L) [12 weeks]

    serum creatinine at final visit - serum creatinine at initial visit

  21. Changes in blood urea nitrogen (mmol/L) [12 weeks]

    blood urea nitrogen at final visit - blood urea nitrogen at initial visit

  22. Changes in serum uric acid (umol/L) [12 weeks]

    serum uric acid at final visit - serum uric acid at initial visit

  23. Changes in proteinuria creatinine ratio (g/g) [12 weeks]

    proteinuria creatinine ratio at final visit - proteinuria creatinine ratio at initial visit

  24. Changes in serum cystatin C (mg/L) [12 weeks]

    serum cystatin C at final visit - serum cystatin C at initial visit

  25. Changes in total urine urea in 24 hours (mmol/24h) [12 weeks]

    total urine urea in 24 hours at final visit - total urine urea in 24 hours at initial visit

  26. Changes in interleukin-6 (pg/mL) [12 weeks]

    interleukin-6 at final visit - interleukin-6 at initial visit

  27. Changes in tumor necrosis factor-α (pg/mL) [12 weeks]

    tumor necrosis factor-α at final visit - tumor necrosis factor-α at initial visit

  28. Changes in C-reactive protein (mg/L) [12 weeks]

    C-reactive protein at final visit - C-reactive protein at initial visit

  29. Changes in species of intestinal flora [12 weeks]

    species of intestinal flora at final visit - species of intestinal flora at initial visit

Other Outcome Measures

  1. Changes in hunger scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  2. Changes in fatigue scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  3. Changes in satiety scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  4. Changes in gastrointestinal flatulence scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  5. Changes in nausea and vomiting scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  6. Changes in constipation scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  7. Changes in diarrhea scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  8. Changes in dry mouth and bitterness scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  9. Changes in dizziness and headache scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  10. Changes in irritability scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  11. Changes in anxiety scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

  12. Changes in depression scores [Weeks 6 and 12]

    Assessed using Visual Analog Scales (VAS with a scale of 1-10)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18-65 years

  • CKD stage 3-4 and not on dialysis (eGFR: 15-59ml/min/1.73m2)

  • BMI ≥ 25 kg/m2

  • Good reading and comprehension skills, simple smartphone operation and no communication difficulties

  • Signed informed consent

Exclusion Criteria:
  • Pregnant and breastfeeding

  • End-stage diseases

  • Acute and active diseases such as gastrointestinal bleeding or acute infections, serious decompensation with diseases such as cirrhosis decompensation stage, malignant tumor, serious heart and lung diseases, severe primary diseases of hematopoietic system, severe hypertension (systolic blood pressure ≥200mmHg, diastolic blood pressure ≥120mmHg) and difficult to control blood pressure, within 3 months after major surgery, such as open surgery

  • Mental patients

  • Using medium-high doses of hormones and immunosuppressants

  • Participating in other researchers

  • Taking other dietary therapies, undergoing weight loss treatment

  • Vegetarian

  • Type 1 diabetes and type 2 diabetes using insulin

Contacts and Locations

Locations

Site City State Country Postal Code
1 Guangdong Provincial Hospital of Chinese Medicine Guangzhou Guangdong China 510120

Sponsors and Collaborators

  • Guangdong Provincial Hospital of Traditional Chinese Medicine

Investigators

  • Study Chair: Xu-sheng Liu, M.M, Guangdong Provincial Hospital of Traditional Chinese Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Liu Xu-sheng, Head of Nephrology, Director, Principal Investigator, Clinical Professor, Guangdong Provincial Hospital of Traditional Chinese Medicine
ClinicalTrials.gov Identifier:
NCT05037747
Other Study ID Numbers:
  • YF2021-142
First Posted:
Sep 8, 2021
Last Update Posted:
Jul 7, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Liu Xu-sheng, Head of Nephrology, Director, Principal Investigator, Clinical Professor, Guangdong Provincial Hospital of Traditional Chinese Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2022