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A single case randomized controlled study of Baduanjin in the treatment of hypertension complicated with anxiety and depression under the concept of "psycho-cardiological harmony"

Effect of Baduanjin on physical and mental health of patients with hypertension complicated with anxiety and depression: a single case randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076301
Enrollment
Unknown
Registered
2023-09-29
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hypertension complicated with anxiety and depression

Interventions

Test group:Baduanjin Exercise/Regular Exercise (First Round) - Washing Period - Regular Exercise/Baduanjin Exercise (Second Round)

Sponsors

First teaching hospital of Tianjin university of traditional Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. aged 35-75 years; 2. meet the level 1 and level 2 eh diagnostic criteria, that is, 140 = SBP < 180mmhg and / or 90 = DBP < 110mmhg; 3. adopt fixed step-down scheme in a long-term rule; 4. those who meet the diagnostic criteria of mild and moderate anxiety and depression, namely 5 = gad-7/phq-9 = 14, and do not take or regularly take anti anxiety and antidepressant drugs for a long time; 5. in good condition, without exercise contraindications, and qualified for Baduanjin or routine exercise; 6. those who voluntarily participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. patients with secondary and rapidly progressive eh; 2. patients with severe diseases such as stroke, diabetes, liver and kidney failure; 3. patients with cognitive impairment or limb dysfunction; 4. patients who have communication difficulties and cannot cooperate; 5. preparing pregnant, pregnant or lactating women; 6. the investigator judged that the patient's compliance was not good and could not complete the trial.

Design outcomes

Primary

MeasureTime frame
Home Blood Pressure Measurement;Self-Rating Anxiety Scale;Self-Rating Depression Scale;

Secondary

MeasureTime frame
Blood pressure and heart rate in consulting room;Symptom score of patients' self-assessment: 7-point Likert scale supplemented by visual analogue scale;Traditional Chinese Medicine syndrome score;

Countries

China

Contacts

Public ContactJingyuan Mao

First teaching hospital of Tianjin university of traditional Chinese medicine

jymao@126.com+86 138 2049 8886

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026