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Effect of Physiotherapy Protocol in Treatment of Depression: Longitudinal Study

Effect of Physiotherapy Protocol in Treatment of Depression: Longitudinal Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05786677
Enrollment
76
Registered
2023-03-27
Start date
2023-04-01
Completion date
2023-08-15
Last updated
2023-03-27

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

Conditions

Depression, Fibromyalgia

Brief summary

The purpose of his study is to investigate the effect of physiotherapy protocol in management of depression in patients with fibromyalgia and in patients with psychogenic depression.

Detailed description

This study will investigate the effect of physiotherapy protocol in management of depression in patients with fibromyalgia and in patients with psychogenic depression.

Interventions

the physiotherapy protocol which will include: 4. Exercise in the form of: d. Breathing exercise e. Aerobic exercise (walking on treadmill with a speed of 3 miles per hour and 0% inclination) f. Bridging exercise 5. Manual techniques in the form of: 1. Suboccipital release 2. Diaphragm release 3. Clavi-pectoral myofascial release 6. Home Routine c. Hot tub bath for 30 minutes d. Breathing exercise

Selective serotonin reuptake inhibitors (SSRIs)

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. Fibromyalgia patients will be included if they meet the diagnosis of FM according to the American College Rheumatology (ACR), diagnosed with depression and referred by a physician. 2. Patients diagnosed with mild and moderate forms of major depression. 3. Their ages range from 20- 60 years old. 4. Patients willing and able to participate in a physiotherapy program and capable of doing physical exercise on their own.

Exclusion criteria

1. severe spinal injuries 2. severe musculoskeletal abnormalities 3. inflammatory rheumatic diseases 4. respiratory or cardiac pathologies 5. Any vestibular, visual or neurological dysfunction affecting balance. 6. History of suicidal attempts 7. Severe depression 8. Suffering from severe somatic or psychiatric disorders.

Design outcomes

Primary

MeasureTime frameDescription
Assessing the change in severity of respondents' depressionat baseline, after 2 weeks of intervention, after 4 weeks of intervention and after one month and two months of end of treatment periodAssessment will be done by using Arabic version of Beck Depression Inventory (BDI) which is designed to rate the severity of respondents' depression in the weeks preceding questionnaire completion. Each of the 21 questions presents four different statements and asks respondents to select the option that best represents them. Statements refer to depressive states in varying degrees of severity (from I do not feel sad to I am so sad or unhappy that I can't stand it), and this is reflected in the scoring process which assigns higher values to responses indicating more acute symptoms of depression. The total score can range from 0 to 63 points, with a total score of 0-9 points indicating minimal depression, 10-18 points mild, 19-29 points moderate, and 30-63 points severe depression.

Countries

Egypt

Contacts

Primary ContactMahitab Momen
bobapt@hotmail.com010226960790
Backup ContactMahitab Momen
bobapt@hotmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026