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Evaluation the effect of jujube and lemon balm extracts in patients with chronic obstructive pulmonary disease

Evaluation the effect of jujube and lemon balm extract accompanying anxiety symptoms and respiratory symptoms in patients with chronic obstructive pulmonary disease (COPD)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220628055302N1
Enrollment
60
Registered
2022-07-23
Start date
2023-01-28
Completion date
Unknown
Last updated
2023-03-13

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

Conditions

Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention 1: Intervention group: Hydroalcoholic extract of jujube and lemonbalm in the form of capsules 750 mg twice a day for 6 weeks. Intervention 2: Control group: placebo(Avisel) capsule for 6

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: People aged 40 to 70 with COPD, whose disease has been confirmed by a lung specialist COPD patients who did not have a known anxiety disorder and were not under standard psychiatric treatment, but had a score of 8 or higher based on the HADS questionnaire People who are satisfied with traditional treatment

Exclusion criteria

Exclusion criteria: Pregnancy and breastfeeding A history of severe anxiety that requires classical medical treatment People who are under the supervision of a psychiatrist or take psychiatric medication due to a known anxiety or mood disorder People who have severe anxiety in the screening tests will be referred to a psychiatrist for diagnostic evaluation and standard treatment Suffering from other medical diseases including hypothyroidism

Design outcomes

Primary

MeasureTime frame
Anxiety score in HADS anxiety subscale questionnaire. Timepoint: At the beginning of the study (before the intervention) and the 3rd and 6th week. Method of measurement: HADS anxiety subscale questionnaire.;Anxiety score in Spielberger's Clear and Hidden Anxiety Questionnaire (STAI). Timepoint: At the beginning of the study (before the intervention) and the 3rd and 6th week. Method of measurement: Spielberger state anxiety questionnaire.;CAT score. Timepoint: At the beginning of the study (before the intervention) and the 3rd and 6th week. Method of measurement: CAT test.

Secondary

MeasureTime frame
Distance traveled in the 6MWT. Timepoint: At the beginning of the study (before the intervention) and the 3rd and 6th. Method of measurement: 6-minute walk test (6MWT).;Number of times sitting and getting up in the chair. Timepoint: At the beginning of the study (before the intervention) and the 3rd and 6th. Method of measurement: 1-min sit-to-stand test (STST).;Blood oxygen saturation (SaO2). Timepoint: At the beginning and end of each round of the (STST) and (6MWT). Method of measurement: Pulse oximeter device.;Pulse rate. Timepoint: At the beginning and end of each round of the (STST) and (6MWT). Method of measurement: Pulse oximeter device.;Quality of Life score on WHO Quality of Life Questionnaire (Bref-WHOQol). Timepoint: Before and after intervention. Method of measurement: WHO Quality of Life Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamane Mousapoor

Mashhad University of Medical Sciences

mousapours981@mums.ac.ir+98 51 3884 8931

Outcome results

None listed

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