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Effect of manual therapy in subjects with cardiovascular disease

Autonomic responses of coronary patients submitted to a protocol of osteopathic techniques: a crossover clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7yqk5p
Enrollment
Unknown
Registered
2019-08-09
Start date
2019-08-15
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Coronary disease

Interventions

Intervention group (number= 18): Treatment of the parietal peritoneum, major omentum, hemodynamic technique for the intestinal loops, pumping of the liver and central tendon. -Technique 1 - Treatment
Other
E02.190.599
E02.190.599.280

Sponsors

Núcleo de Pesquisa do Instituto Docusse de Osteopatia e Terapia Manual
Lead Sponsor
Núcleo de Pesquisa do Instituto Docusse de Osteopatia e Terapia Manual
Collaborator

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Men with a diagnosis of ischemic coronary disease; above 45 years of age; who do not present a history of smoking or alcoholism; cardiovascular rehabilitation program followers who do not present a historical recruitment period for infections; do not present with unstable angina; controlled hypertension; without significant valvular disease; without uncontrolled metabolic disease

Exclusion criteria

Exclusion criteria: Volunteers will be excluded from the study when time series records of RR intervals show less than 95% of sinus beats; absence of attendance in at least one of the stages of the study

Design outcomes

Primary

MeasureTime frame
Outcome expected 1 The autonomic behavior will be evaluated by analyzing the heart rate variability determined at the beginning and end of the care. An increase in the measures of heart rate variability is expected for the indices that evaluate the parasympathetic autonomic behavior (RMSSD, HF, SD1), immediately after the intervention protocol.

Secondary

MeasureTime frame
Outcome expected 2 Cutaneous temperature through the thermographic camera  The outcome will be assessed pre and post intervention. Reduction of cutaneous temperature is expected immediately after the intervention protocol is performed.;Outcome expected 3 Blood pressure through the sphygmomanometer and stethoscope The outcome will be assessed pre and post intervention. Reduction of blood pressure is expected immediately after the intervention protocol is performed.;Outcome expected 4 Heart rate through the heart monitor.  The outcome will be assessed pre and post intervention. Reduction of heart rate is expected immediately after the intervention protocol is performed.

Countries

Brazil

Contacts

Public ContactGuilherme Luchesi

Núcleo de Pesquisa do Instituto Docusse de Osteopatia e Terapia Manual

gui.luchesi@hotmail.com+55 18 3222 4245

Outcome results

None listed

Source: REBEC (via WHO ICTRP)