YACHT: Yoga And Cardiovascular Health Trial

Sponsor
Imperial College London (Other)
Overall Status
Completed
CT.gov ID
NCT01597960
Collaborator
London School of Hygiene and Tropical Medicine (Other)
80
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2
10
8

Study Details

Study Description

Brief Summary

The benefits of alternative therapeutic approaches, such as yoga, are poorly understood and this is particularly true of the beneficial effects on cardiovascular disease (CVD) risk. It is hoped that a better understanding of the value of this therapy will provide a sound scientific basis for including yoga in mainstream clinical practice. The investigators propose to study a group of 80 participants (40 Indian Asians and 40 Europeans) recruited from a cardiac rehabilitation programme in West London post-angioplasty as treatment for an acute coronary syndrome. Those who agree will undergo a series of baseline and follow-up measurements. 20 Indian Asians and 20 Europeans will be randomized to the yoga intervention plus their standard cardiac rehabilitation programme (usual care), and the remaining 20 Indian Asians and 20 Europeans will be randomized to usual care alone. Baseline and follow-up measurements will be performed on all participants. In order to determine the acute effects of yoga the group randomised to the yoga intervention will also undergo a series of acute tests before and after their first yoga session.

Condition or Disease Intervention/Treatment Phase
  • Other: Yoga
N/A

Detailed Description

The benefits of alternative therapeutic approaches, such as yoga, are poorly understood and this is particularly true of the beneficial effects on cardiovascular disease (CVD) risk. It is hoped that a better understanding of the value of this therapy will provide a sound scientific basis for including yoga in mainstream clinical practice. The investigators propose to study a group of 80 participants (40 Indian Asians and 40 Europeans) recruited from a cardiac rehabilitation programme in West London post-angioplasty as treatment for an acute coronary syndrome. Those who agree will undergo a series of baseline and follow-up measurements. 20 Indian Asians and 20 Europeans will be randomized to the yoga intervention plus their standard cardiac rehabilitation programme (usual care), and the remaining 20 Indian Asians and 20 Europeans will be randomized to usual care alone. Baseline and follow-up measurements will be performed on all participants; these include: Demographic & health questionnaire, Lifestyle questionnaires focusing on diet and exercise, Fasting bloods sampling (for cardiovascular risk factors and markers), Saliva sampling (x 5 samples for salivary cortisol and alpha-amylase), Anthropometrics - height, weight and waist and hip circumference, Bioimpedence - measurement of total body fat, 3D and Doppler echocardiography, Carotid IMT, Resting brachial blood pressure, Central blood pressure (tonometery at the radial artery), Pulse Wave Velocity, 12 lead ECG, Cardiopulmonary exercise testing, Combined 24hr BP & ECG monitor, Accelerometer (3 days). In order to determine the acute effects of yoga the group randomised to the yoga intervention will also undergo a series of acute tests before and after their first yoga session. These include: Exercise capacity, Saliva sampling (x 5 samples for salivary cortisol and alpha-amylase) and combined 24hr BP & ECG monitor.

Study Design

Study Type:
Interventional
Actual Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Yoga And Cardiovascular Health Trial
Study Start Date :
Jun 1, 2012
Actual Primary Completion Date :
Apr 1, 2013
Actual Study Completion Date :
Apr 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Yoga 12 week programme

Usual care (standard cardiac rehabilitation programme) plus yoga intervention.

Other: Yoga
Those randomised to usual care plus the yoga intervention will be required to attend yoga classes twice a week for 12 weeks alongside their cardiac rehabilitation programme. There will be 24 yoga classes in total, of which, we require the participant to attend a minimum of 18. The yoga classes will be conducted by a teacher certified in yoga and cardiac rehabilitation and will encompass physical fitness (yoga poses), stress reduction (breath control and meditation) and positive lifestyle changes (diet, smoking and alcohol).

No Intervention: Usual care

Usual care (standard cardiac rehabilitation programme) only.

Outcome Measures

Primary Outcome Measures

  1. Cardiopulmonary function [Week 0 (pre intervention) and week 12 (post intervention)]

    To perform a mechanistic study that determines the acute and chronic effects of yoga on cardiopulmonary function, autonomic function, blood pressure and heart rate.

Secondary Outcome Measures

  1. Blood pressure [Week 0 (pre intervention), week 1 (pre & post 1st yoga class), and week 12 (post intervention)]

    Blood pressure will be measured at baseline, at the beginning and end of the first yoga class, and immediately after the 12 week intervention.

  2. Heart rate and heart rate variability [Week 0 (pre intervention), week 1 (pre & post 1st yoga class), and week 12 (post intervention)]

    Heart rate and heart rate variability will be measured at baseline, at the beginning and end of the first yoga class, and immediately after the 12 week intervention.

  3. Stress hormones [Week 0 (pre intervention), week 1 (pre & post 1st yoga class), and week 12 (post intervention)]

    Stress hormones will be measured at baseline, at the beginning and end of the first yoga class, and immediately after the 12 week intervention.

  4. Exercise capacity [Week 0 (pre intervention), week 1 (pre & post 1st yoga class), and week 12 (post intervention)]

    Exercise capacity will be measured at baseline, at the beginning and end of the first yoga class, and immediately after the 12 week intervention.

  5. Body fat [Week 0 (pre intervention) and week 12 (post intervention)]

    Body fat will be measured at baseline and immediately after the 12 week intervention.

  6. Glucose and lipids [Week 0 (pre intervention) and week 12 (post intervention)]

    Glucose and lipids will be measured at baseline and immediately after the 12 week intervention.

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged 35-80 years.

  • Male or female.

  • European or Indian Asian descent.

  • Able to understand English or Punjabi.

  • Referred to a cardiac rehabilitation programme in West London post-angioplasty as treatment for an acute coronary syndrome.

Exclusion Criteria:
  • Adults under 35 years or above 80 years.

  • Adults aged 35-80 years who are not competent to give consent.

  • Co-morbid disease or mobility limitations that would preclude participation in cardiac rehabilitation and our investigations.

Contacts and Locations

Locations

Site City State Country Postal Code
1 International Centre for Circulatory Health London United Kingdom W2 1LA

Sponsors and Collaborators

  • Imperial College London
  • London School of Hygiene and Tropical Medicine

Investigators

  • Principal Investigator: Nishi Chaturvedi, Imperial College London

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Imperial College London
ClinicalTrials.gov Identifier:
NCT01597960
Other Study ID Numbers:
  • 12/LO/0597
First Posted:
May 15, 2012
Last Update Posted:
Nov 11, 2016
Last Verified:
Jun 1, 2012
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 11, 2016