Heat-sensitive Moxibustion Self-administration in Patients in the Community With Primary Hypertension: Protocol for a Multi-center, Pragmatic, Non-randomized Trial

Sponsor
Jiangxi University of Traditional Chinese Medicine (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04381520
Collaborator
Nangang community healthcare center (Nanchang city, Jiangxi province, China) (Other), Honggutan community healthcare center (Nanchang city, Jiangxi province, China) (Other), Shengmi community healthcare center (Nanchang city, Jiangxi province, China) (Other), Gaofu town community healthcare center (Fu Zhou city, Jiangxi province, China) (Other)
767
1
2
13.3
57.5

Study Details

Study Description

Brief Summary

Heat-sensitive moxibustion is considered to be effective for primary hypertension in hospital setting. This study aims to investigate whether heat-sensitive moxibustion self-administration is effective for lowering blood pressure and improving quality of life for patients with primary hypertension in community setting using a multicenter, prospective, non-randomized study design

Condition or Disease Intervention/Treatment Phase
  • Other: Heat-sensitive moxibustion plus antihypertensive drugs
  • Drug: Antihypertensive drugs
N/A

Detailed Description

Primary hypertension is a global health issue with high incidence; it affected approximately 1.13 billion people worldwide and directly or indirectly causing an 10.4 million of death yearly. The routine drugs for primary hypertension are limited by adverse effects and expensive costs. Therefore, complementary and alternative medicine with good efficacy and safety and low expenditure is still needed for primary hypertension, especially in poverty-stricken areas.

Heat-sensitive moxibustion is an innovative therapy developed on the basis of traditional moxibustion. Compared with traditional moxibustion, heat-sensitive moxibustion advocates finding heat-sensitive acupoints where patients have special reactions to moxibustion heat, including diathermy, heat transfer, soreness, etc. The application of moxibustion on heat-sensitive acupoints (i.e., heat-sensitive moxibustion) has been shown to be more effective to traditional moxibustion for many diseases, including primary hypertension. Moreover, compared with acupuncture, heat-sensitive moxibustion has a main advantage that moxibustion does not require professional qualifications and patients can self-administer moxibustion after professional training. However, the current evidence is generated only from hospital settings. Therefore, this study is specifically designed to investigate whether heat-sensitive moxibustion self-administration is an effective intervention for lowering blood pressure and improving quality of life for patients with primary hypertension in community setting.

Study Design

Study Type:
Interventional
Actual Enrollment :
767 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Heat-sensitive Moxibustion Self-administration in Patients in the Community With Primary Hypertension: Protocol for a Multi-center, Pragmatic, Non-randomized Trial
Actual Study Start Date :
May 20, 2020
Anticipated Primary Completion Date :
Jun 30, 2021
Anticipated Study Completion Date :
Jun 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Heat-sensitive moxibustion plus antihypertensive drugs

Other: Heat-sensitive moxibustion plus antihypertensive drugs
In this arm, patients will administer heat-sensitive moxibustion by themselves or by the help of their family after professional training. Patients will maintain their original antihypertensive drugs. The periods of treatment and follow-up will be one year.

Active Comparator: Antihypertensive drugs

Drug: Antihypertensive drugs
In this arm, patients will maintain their original antihypertensive drugs. The periods of treatment and follow-up will be one year.

Outcome Measures

Primary Outcome Measures

  1. Changes in systolic blood pressure (mmHg) [Baseline, 6 months, and 12 months]

  2. Changes in diastolic blood pressure (mmHg) [Baseline, 6 months, and 12 months]

  3. Changes in dose of antihypertensive drugs [Baseline, 6 months, and 12 months]

    Measured by percentage changes

Secondary Outcome Measures

  1. Total score of quality of life assessed by a validated patient-reported outcome scale [Baseline, 6 months, and 12 months]

    Including 27 items and assessing impacts of hypertension on on the three dimensions, physical (18 items), psychological (4 items) and family-social (5 items). Each item is classified as five grades (0-4 points). The total score ranges from 0 to 108 points. A higher score indicates a worse quality of life.

  2. Physical score of quality of life assessed by a validated patient-reported outcome scale [Baseline, 6 months, and 12 months]

    Including 18 items. Each item is classified as five grades (0-4 points). The total score ranges from 0 to 72 points. A higher score indicates a worse quality of life.

  3. Psychological score of quality of life assessed by a validated patient-reported outcome scale [Baseline, 6 months, and 12 months]

    Including 4 items. Each item is classified as five grades (0-4 points). The total score ranges from 0 to 16 points. A higher score indicates a worse quality of life.

  4. Family-social score of quality of life assessed by a validated patient-reported outcome scale [Baseline, 6 months, and 12 months]

    Including 5 items. Each item is classified as five grades (0-4 points). The total score ranges from 0 to 20 points. A higher score indicates a worse quality of life.

  5. Changes in fasting blood glucose (mg/dl) [Baseline, 6 months, and 12 months]

  6. Changes in glycated hemoglobin (%) [Baseline, 6 months, and 12 months]

  7. Changes in total cholesterol (mg/dl) [Baseline, 6 months, and 12 months]

  8. Changes in triglycerides (mg/dl) [Baseline, 6 months, and 12 months]

  9. Changes in low density lipoprotein cholesterol (mg/dl) [Baseline, 6 months, and 12 months]

  10. Changes in high density lipoprotein cholesterol (mg/dl) [Baseline, 6 months, and 12 months]

  11. Changes in urinary albumin (g/l) [Baseline, 6 months, and 12 months]

  12. Changes in serum creatinine (μmol/l) [Baseline, 6 months, and 12 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Meet the diagnostic criteria of primary hypertension

  2. 18 to 70 years old

  3. Sign the informed consent

Exclusion Criteria:
  1. Secondary hypertension caused by kidney disease, macrovascular disease, pregnancy, endocrine disease, brain disease, drug-induced factors, etc.

  2. Allergic to moxibustion equipment, moxa smoke or moxa

  3. Pregnancy or lactation

  4. A history of serious cardiovascular and cerebrovascular events such as cerebrovascular accidents and myocardial infarction

  5. Complicated by liver and kidney dysfunction indicated by total bilirubin, alanine aminotransferase, aspartate aminotransferase, or blood creatinine are more than 2 times upper limit of normal value

  6. Complicated by malignant tumors

  7. Complicated by major mental disorders

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jiangxi University of Traditional Chinese Medicine Nanchang Jiangxi China 330004

Sponsors and Collaborators

  • Jiangxi University of Traditional Chinese Medicine
  • Nangang community healthcare center (Nanchang city, Jiangxi province, China)
  • Honggutan community healthcare center (Nanchang city, Jiangxi province, China)
  • Shengmi community healthcare center (Nanchang city, Jiangxi province, China)
  • Gaofu town community healthcare center (Fu Zhou city, Jiangxi province, China)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xu Zhou, Associate professor, Jiangxi University of Traditional Chinese Medicine
ClinicalTrials.gov Identifier:
NCT04381520
Other Study ID Numbers:
  • JXUTCM-Mox-01
First Posted:
May 11, 2020
Last Update Posted:
Apr 5, 2021
Last Verified:
Apr 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 5, 2021