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Intervention Effect of Shen-based Qigong Exercise on Residual Symptoms of Schizophrenia

Discussion on the Intervention Effect of Shen-based Qigong Exercise on Residual Symptoms of Schizophrenia Based on the Theory of Heart Dominating Mind and Body-spirit Syncretism in Traditional Chinese Medicine

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05310955
Enrollment
60
Registered
2022-04-05
Start date
2022-08-16
Completion date
2023-06-30
Last updated
2022-10-26

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

Conditions

Schizophrenia

Brief summary

The purpose of this study is to observe the intervention effect of shen-based Qigong exercise on residual symptoms of schizophrenia.

Detailed description

Shen-based Qigong exercise is a new kind of health-care Qigong exercise based on the theory of traditional Chinese medicine, aiming at the characteristics of schizophrenia. In this study, a randomized controlled trial was conducted to observe the rehabilitation effect of this new exercise on residual symptoms of schizophrenic patients. Questionnaire, test and other experimental materials were used to evaluate the intervention effect of 12-week shen-based Qigong exercise on psychiatric symptoms, cognitive function, quality of life and social function of schizophrenic patients. At the same time, the related physical function and cardiac function indexes were used to evaluate the physical and cardiac rehabilitation effects of the exercise on patients from the aspects of body and heart, so as to verify whether Qigong exercise has the effects of adjusting body and heart.

Interventions

OTHERdaily rehabilitation interventions

including Naikan therapy, Morita therapy, group art therapy, group painting therapy

OTHERshen-based Qigong exercise

a 12-week intervention of shen-based Qigong exercise : exercise 5 days a week, about 30 minutes a day

Sponsors

Shanghai University of Traditional Chinese Medicine
CollaboratorOTHER
Shanghai Mental Health Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Han Chinese population 2. age ≥ 18 years 3. education level ≥ 6 years, can fill in the questionnaire independently, have enough audio-visual level to complete the necessary examination 4. assessed by MINI 7.0 and satisfied with the diagnostic criteria for schizophrenia based on the Diagnostic and Statistical Manual of Mental Disorders, fifth edition(DSM-5) 5. patients with schizophrenia residing in the rehabilitation ward, without relapse in the past 6 months 6. residual negative symptoms, with at least one item ≥ 2 on the negative subscale of PANSS (N1-N7) 7. taking second generation antipsychotics 8. no training history of traditional Chinese exercises 9. agreement to participate in the study and willing to give written informed consent

Exclusion criteria

1. having severe physical diseases such as cardiovascular, lung, liver, kidney, and hematopoietic diseases 2. satisfied with the diagnostic criteria for other mental disorders based on DSM-5 3. having alcohol or substance abuse/dependence 4. having mental retardation(WAIS\<70) and/or severe cognitive impairment(MMSE\<24) 5. having visual and / or hearing problems, unable to complete the relevant test 6. electroconvulsive or repetitive transcranial magnetic stimulation(rTMS) therapy in the past 3 months 7. currently enrolled or participated in other clinical studies in the past 3 months 8. participating in regular exercise training in the past 6 months 9. failure to sign or refuse to sign informed consent

Design outcomes

Primary

MeasureTime frameDescription
change of the Scale for the Assessment of Negative Symptoms (SANS)Change from Baseline at 3 monthsNegative symptoms will be evaluated using the Scale for the Assessment of Negative Symptoms (SANS). The scale made up for the lack of attention to negative symptoms in previous psychiatric rating scales. It contains five subscales: affective blunting, alogia, avolition/apathy, anhedonia/asociality, and attention. A total of 24 items were scored at 6 levels for each item.

Secondary

MeasureTime frameDescription
change of Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)Change from Baseline at 3 monthsRBANS will be used to assess global cognitive function. RBANS yields scaled scores for 5 cognitive domains and shows a good effect in cognitive assessment of patients with schizophrenia.
change of event-related potential P300 (ERP P300)Change from Baseline at 3 monthsERP P300 will be used to assess global cognitive function. ERP P300 is an endogenous cognitive component related to high-level psychological activities such as attention, memory, feeling, learning and reasoning. It has good stability and can reflect the level of cognitive function from different aspects.

Other

MeasureTime frameDescription
change of the Scale for the Assessment of Positive Symptoms (SAPS)Change from Baseline at 3 monthsPositive symptoms will be evaluated using the Scale for the Assessment of Positive Symptoms (SAPS). SAPS measures positive symptoms on a 34 item, 6-point scale, a total of 170 points. Items are listed under hallucinations, delusions, bizarre behavior, and positive formal thought disorder.
change of heart rate variability (HRV)Change from Baseline at 3 monthsHeart rate variability (HRV) will be used as the evaluation index for cardiac function. HRV is a widely used non-invasive tool for evaluating cardiac autonomic nerve function.
change of heightChange from Baseline at 3 monthsHeight will be measured using a height ruler, expressed in meters.
change of n-back taskChange from Baseline at 3 monthsSpecific cognitive domain--working memory will be assessed by n-back task. N-back task paradigm is the most classical paradigm in working memory research.
change of waistlineChange from Baseline at 3 monthsWaistline will be measured using a flexible rule, expressed in centimeters.
change of blood pressureChange from Baseline at 3 monthsBlood pressure will be measured using a sphygmomanometer, expressed in millimeter of mercury.
change of gait dataChange from Baseline at 3 monthsAcquire gait data in a quiet, well-lit room. Specify the walking area to guide the participants to complete the walking cycle.
change of weightChange from Baseline at 3 monthsWeight will be measured using a weighting scale, expressed in kilograms.
change of 36-item Short Form Health Survey(SF-36)Change from Baseline at 3 months36-item Short Form Health Survey(SF-36)will be used to assess the health-related quality of life of patients. SF-36 is one of the most commonly used standardized measurement tools for quality of life in the world, including eight subscales, a total of 36 items, involving physical and mental health.
change of Social-Adaptive Functioning Evaluation (SAFE)Change from Baseline at 3 monthsSocial functions will be assessed using Social-Adaptive Functioning Evaluation (SAFE). SAFE can evaluate the social adaptation function of patients with mental disorders over 18 years old. It has a total of 19 items, divided into basic life skills, advanced life skills, social skills and communication skills in four areas; each item 0-4 score, the higher the score, the more serious the damage.

Countries

China

Contacts

Primary ContactAnbei Lian
782115188@qq.com18117205070

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026