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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05528146
Other study ID # Hungkuang University
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 1, 2022
Est. completion date August 31, 2023

Study information

Verified date September 2022
Source Hungkuang University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Constipation in schizophrenia is an important issue in clinical care. Constipation needs psychiatric professionals concerning and providing intervention because it may cause ileus and lead to death. The cause of constipation in patients may be due to side effects of antipsychotic medication, sedentary lifestyle, insufficient water intake, fiber, etc. The study aims to increase fiber of the consumption of psyllium to assess the constipation effectiveness in schizophrenics. The study conducted a crossover research design. G-power was used to calculate the 22 subjects in each of the two groups. A total of 44 patients with constipation who were schizophrenics will participate in the study. Patients will use simple randomly to be divided into two groups based on their live ward for pre-testing. These two groups will receive either psyllium 3.5 g/day or 7 g/day for 4 weeks in a single-blind, crossover trial. The trial will stop 1week after the first phase and post-test. Then, two groups will exchange the dose for 4 weeks. Post-test will record after finishing this second phase trial. This study can understand the benefits of psyllium on schizophrenics with constipation symptoms and can give professional suggestions to patients with constipation in the future.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 44
Est. completion date August 31, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: 1. DSM-V was diagnoses with schizophrenia inpatients. 2. Aged between 20 years and above. 3. Those who defecate less than 3 times a week, or those who have Bristol stool form scale between 1 and 2, or those who have constipation assessment scale (CAS) scores more than one point from questions 3 to 8; Or use PRN stool softeners (including oral and suppository) at least once a week. 4. Clear awareness and able to communicate in Chinese and Taiwanese. Exclusion Criteria: 1. Patients with intestinal diseases such as colon cancer, irritable bowel syndrome and other organic intestinal diseases such as rectal bleeding, intestinal surgery, rectal prolapse and other medical history. 2. Cases with positive fecal occult blood test in the past six months, changes in stool thickness for one month, history of iron deficiency anemia, and unexplained weight loss for one month. 3. Those who are unable to cooperate due to obvious mental symptoms. 4. History of grain allergy, asthma.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Psyllium huks
psyllium in 250ml of water

Locations

Country Name City State
Taiwan Changhua Hospitol Chang Hua Puxin Township

Sponsors (1)

Lead Sponsor Collaborator
Hungkuang University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Other Constipation Assessment Scale, CAS improved constipation symptoms 4weeks
Primary bowel movement increased stool frequency 4weeks
Secondary Stool type improved stool type (bristol stool form) 4weeks
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