The Effect of HIT in Patients With Non-alcoholic Fatty Liver Disease/Steatohepatitis
Primary Purpose
Non-alcoholic Steatohepatitis, Non-alcoholic Fatty Liver Disease
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
High-intensity Interval Training
Sponsored by
About this trial
This is an interventional treatment trial for Non-alcoholic Steatohepatitis focused on measuring High-intensity Interval Training
Eligibility Criteria
Inclusion Criteria:
- clinical diagnosis of non-alcoholic fatty liver disease or non-alcoholic steatohepatitis
- attending a specialist liver clinic at Ninewells Hospital, Dundee
Exclusion Criteria:
- unstable cardiovascular disease
- uncontrolled arrhythmias
- structural cardiac abnormalities
- uncontrolled diabetes
- other uncontrolled metabolic abnormalities
- severe orthopaedic condition that would prohibit exercise
- severe pulmonary condition that would prohibit exercise
- any other poorly controlled medical condition.
- resting systolic blood pressure above 160 mm Hg
- resting diastolic blood pressure above 90 mm Hg
- symptomatic postural drop in blood pressure greater than 20 mm Hg
Sites / Locations
- Abertay University
- Ninewells Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
High-intensity Interval Training (HIT)
Arm Description
6 week control period with no intervention then 6 weeks of twice weekly HIT
Outcomes
Primary Outcome Measures
Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)
calculation of insulin resistance via formula: fasting insulin (mIU/L) x fasting glucose (mg/dL)/405 normal insulin resistance -HOMA score <3 moderate insulin resistance -HOMA score 3-5 severe insulin resistance -HOMA score >5 Assessed at baseline, after 6 week control period and within 1 week of completing 6 weeks HIT
Oral Glucose Tolerance Test
measurement of capillary samples for glucose at time 0, followed by every 20 minutes for 2 hours following ingestion of 75g glucose. Results graphed against time, then area under the curve calculated for each of the 3 assessments.
AST: ALT Ratio
ratio of liver enzymes aspartate aminotransferase (AST) to alanine aminotransferase (ALT).
used as a diagnostic aid e.g. AST:ALT of more than 2:1 is characteristic of alcoholic liver disease whereas fatty steatosis and many other causes of liver disease, ratio is less than or equal to 1.
Ratio may rise as fibrosis and cirrhosis develop in viral hepatitis.
FIB-4
calculated from AST, ALT, platelets and participant's age and used to estimate amount of fibrosis in liver.
Fib-4 score of <1.45 has negative predictive value of 90% for advanced fibrosis.
Body Fat Mass Estimated Via Bioimpedance
total body fat and trunk fat estimated via bioimpedance measured after overnight fast, expressed as percentage
Blood Pressure
taken with participant supine, measured on left arm
General Well-being as Assessed by SF-36 Questionnaire
Assessment of: physical functioning, social functioning, mental health, pain, change in health, physical role limitation, mental role limitation, energy and vitality, health perception over preceding 4 weeks (other than change in health, which is a comparison to health the preceding year), expressed as a transformed score range 0-100, with a higher score indicating better function/freedom from pain etc
Short-term Memory Recall
testing of verbal word presentation-immediate recall of 10 words (60 seconds for recall) Maximum =10, minimum =0
Estimated VO2 Max
VO2 max estimated via submaximal exercise test-submaximal treadmill walking test Calculated via formula: VO2max= 15.1+21.8 x speed (miles per hour) - 0.327 x heart rate (beats per minute) - 0.263 x speed x age (years) + 0.00504 x heart rate x age + 5.98 x gender (0=female, 1=male)
Physical Function-"Get up and go" Test
participant will be timed standing up from chair unaided,walking 30m, turning round and returning to a seated position on the chair, the average time of 3 attempts will be recorded.
Ankle Brachial Pressure Index (ABPI)
ratio of blood pressure in left arm and right ankle
Long-term Memory Recall
testing of verbal word presentation-delayed recall of 10 words 10 minutes after words initially presented (within 60 seconds).
Maximum= 10 words, minimum = no words
Executive Function (Verbal Fluency Test)
written verbal fluency test: participant asked to write down as many English words as possible within 60 seconds, starting with a particular letter of the alphabet, excluding proper nouns or plurals.
Baseline assessment-letter A Post Control assessment -letter S After HIT assessment -letter F
Secondary Outcome Measures
Full Information
NCT ID
NCT02528305
First Posted
August 10, 2015
Last Updated
May 3, 2018
Sponsor
University of Bath
Collaborators
Abertay University
1. Study Identification
Unique Protocol Identification Number
NCT02528305
Brief Title
The Effect of HIT in Patients With Non-alcoholic Fatty Liver Disease/Steatohepatitis
Official Title
A Pilot Project to Assess the Effect of High-intensity Interval Training in Patients With Non-alcoholic Fatty Liver Disease/Steatohepatitis
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bath
Collaborators
Abertay University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This pilot study aims to investigate whether 6 weeks of twice weekly High-intensity Interval Training (HIT) results in improvements in disease-specific measures, feelings of general well-being, physical fitness and cognitive function in patients with non-alcoholic fatty liver disease or non-alcoholic steatohepatitis.
Detailed Description
The study aims to recruit up to 12 patients diagnosed with non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH) from the liver clinics at Ninewells Hospital, Dundee. Suitable patients who give informed consent will be assessed at baseline, again after 6 weeks of no intervention to act as a control period, and thirdly after 6 weeks of twice-weekly high-intensity interval training (HIT).
Assessments will be performed with the patient fasted overnight, and will involve body composition measurements, blood pressure, a venous blood sample for circulating triglycerides, fasting glucose, insulin, liver enzymes alanine aminotransferase (ALT) and aspartate aminotransferase (AST), and platelets. An oral glucose tolerance test will be performed using fingerprick capillary samples. Cognitive function tests for episodic memory, executive function and semantic memory will be performed and a questionnaire (SF-36) will be used to assess general well-being. Physical fitness will be assessed through a 12-minute walk test on a treadmill, which will allow estimation of maximal oxygen uptake capacity (VO2 max), and a "get up and go" test will be used to assess physical function.
The exercise intervention will involve a 2 minute warm-up, cycling at 50 rpm before the participants will be asked to cycle at 100rpm and a weight will be added (7% body weight for men and 6% body weight for women) as resistance. The sprint will last 6 seconds and the participant will be asked to rest for at least 1 minute. This will be repeated for a total of 5 sprints in sessions 1-3, 6 sprints in session 4, 7 sprints in sessions 5&6, 8 sprints in sessions 7&8, 9 sprints in sessions 9&10 and 10 sprints in sessions 11&12. Exercise heart rate will be monitored and recorded.
At least 3 days after the last HIT session the pre-intervention testing assessment will be repeated for a third time.
Changes in measured variables will be analysed via repeated measures analysis of variance (ANOVA) with post-hoc testing of all variables.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-alcoholic Steatohepatitis, Non-alcoholic Fatty Liver Disease
Keywords
High-intensity Interval Training
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
No Masking, this was not possible with this study design.
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
High-intensity Interval Training (HIT)
Arm Type
Experimental
Arm Description
6 week control period with no intervention then 6 weeks of twice weekly HIT
Intervention Type
Other
Intervention Name(s)
High-intensity Interval Training
Other Intervention Name(s)
Exercise
Intervention Description
2 minute warm-up at 50rpm, then increase to 100rpm. Weight added to bike (7% body weight for men 6% body weight for women). Continue effort for 6 seconds, then passive rest for at least 1 minute. Total 5 sprints in sessions 1-3, 6 sprints in session4, 7 sprints in sessions 5&6, 8 sprints in sessions 7&8, 9 sprints in sessions 9&10 and 10 sprints in sessions 11&12.
Primary Outcome Measure Information:
Title
Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)
Description
calculation of insulin resistance via formula: fasting insulin (mIU/L) x fasting glucose (mg/dL)/405 normal insulin resistance -HOMA score <3 moderate insulin resistance -HOMA score 3-5 severe insulin resistance -HOMA score >5 Assessed at baseline, after 6 week control period and within 1 week of completing 6 weeks HIT
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Oral Glucose Tolerance Test
Description
measurement of capillary samples for glucose at time 0, followed by every 20 minutes for 2 hours following ingestion of 75g glucose. Results graphed against time, then area under the curve calculated for each of the 3 assessments.
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
AST: ALT Ratio
Description
ratio of liver enzymes aspartate aminotransferase (AST) to alanine aminotransferase (ALT).
used as a diagnostic aid e.g. AST:ALT of more than 2:1 is characteristic of alcoholic liver disease whereas fatty steatosis and many other causes of liver disease, ratio is less than or equal to 1.
Ratio may rise as fibrosis and cirrhosis develop in viral hepatitis.
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
FIB-4
Description
calculated from AST, ALT, platelets and participant's age and used to estimate amount of fibrosis in liver.
Fib-4 score of <1.45 has negative predictive value of 90% for advanced fibrosis.
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Body Fat Mass Estimated Via Bioimpedance
Description
total body fat and trunk fat estimated via bioimpedance measured after overnight fast, expressed as percentage
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Blood Pressure
Description
taken with participant supine, measured on left arm
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
General Well-being as Assessed by SF-36 Questionnaire
Description
Assessment of: physical functioning, social functioning, mental health, pain, change in health, physical role limitation, mental role limitation, energy and vitality, health perception over preceding 4 weeks (other than change in health, which is a comparison to health the preceding year), expressed as a transformed score range 0-100, with a higher score indicating better function/freedom from pain etc
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Short-term Memory Recall
Description
testing of verbal word presentation-immediate recall of 10 words (60 seconds for recall) Maximum =10, minimum =0
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Estimated VO2 Max
Description
VO2 max estimated via submaximal exercise test-submaximal treadmill walking test Calculated via formula: VO2max= 15.1+21.8 x speed (miles per hour) - 0.327 x heart rate (beats per minute) - 0.263 x speed x age (years) + 0.00504 x heart rate x age + 5.98 x gender (0=female, 1=male)
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Physical Function-"Get up and go" Test
Description
participant will be timed standing up from chair unaided,walking 30m, turning round and returning to a seated position on the chair, the average time of 3 attempts will be recorded.
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Ankle Brachial Pressure Index (ABPI)
Description
ratio of blood pressure in left arm and right ankle
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Long-term Memory Recall
Description
testing of verbal word presentation-delayed recall of 10 words 10 minutes after words initially presented (within 60 seconds).
Maximum= 10 words, minimum = no words
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
Title
Executive Function (Verbal Fluency Test)
Description
written verbal fluency test: participant asked to write down as many English words as possible within 60 seconds, starting with a particular letter of the alphabet, excluding proper nouns or plurals.
Baseline assessment-letter A Post Control assessment -letter S After HIT assessment -letter F
Time Frame
Baseline, Follow up at 6 Weeks and following HIT intervention at 12 Weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
clinical diagnosis of non-alcoholic fatty liver disease or non-alcoholic steatohepatitis
attending a specialist liver clinic at Ninewells Hospital, Dundee
Exclusion Criteria:
unstable cardiovascular disease
uncontrolled arrhythmias
structural cardiac abnormalities
uncontrolled diabetes
other uncontrolled metabolic abnormalities
severe orthopaedic condition that would prohibit exercise
severe pulmonary condition that would prohibit exercise
any other poorly controlled medical condition.
resting systolic blood pressure above 160 mm Hg
resting diastolic blood pressure above 90 mm Hg
symptomatic postural drop in blood pressure greater than 20 mm Hg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Niels BJ Vollaard, PhD
Organizational Affiliation
University of Bath
Official's Role
Principal Investigator
Facility Information:
Facility Name
Abertay University
City
Dundee
ZIP/Postal Code
DD1 1HG
Country
United Kingdom
Facility Name
Ninewells Hospital
City
Dundee
ZIP/Postal Code
DD1 9SY
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
There is no reason to share the IPD.
Learn more about this trial
The Effect of HIT in Patients With Non-alcoholic Fatty Liver Disease/Steatohepatitis
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