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Comparison of the Effectiveness of Eight Weeks of Selected Corrective Exercises With and Without Self-Hypnosis on Lumbar Lordosis, Low Back Pain Intensity, and Quality of Life in Primiparous Women After Childbirth.

Comparison of the Effectiveness of Eight Weeks of Selected Corrective Exercises With and Without Self-Hypnosis on Lumbar Lordosis, Low Back Pain Intensity, and Quality of Life in Primiparous Women After Childbirth.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250305064939N1
Enrollment
45
Registered
2025-06-11
Start date
2025-06-22
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Condition 1: Low Back pain severity. Condition 2: Degree of lumbar lordosis. Low back pain Postural lordosis

Interventions

Intervention 1: First intervention group: This group receives only selected corrective exercises that have been selected through study, references, and valid articles for 8 weeks, 3 sessions per week

Sponsors

Imam Reza International University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Primiparous women who delivered their first child between 6 weeks and 24 months prior to the study A history of full-term pregnancy (defined as 37 to 42 weeks of gestation) Women aged 18 years or older Confirmed diagnosis of hyperlordosis during the initial evaluation Chronic low back pain (for at least 3 months) Medical clearance for physical activity by the treating physician Willingness to participate in the exercise program Willingness to engage in self-hypnosis as part of the intervention Minimum education level: high school diploma

Exclusion criteria

Exclusion criteria: Presence of severe musculoskeletal disorders Current pregnancy or intention to become pregnant during the course of the study Presence of severe chronic medical conditions that could influence the study outcomes (such as rheumatoid arthritis, advanced osteoporosis, or uncontrolled hypertension) History of spinal surgery

Design outcomes

Primary

MeasureTime frame
Low back pain severity. Timepoint: Prior to the intervention and two months following its initiation. Method of measurement: Visual Analogue Scale and the Quebec back pain disability scale.;Lumbar lordosis angle. Timepoint: Prior to the intervention and two months following its initiation. Method of measurement: 60 cm flexible ruler for measuring spinal curves.;General quality of life. Timepoint: Prior to the intervention and two months following its initiation. Method of measurement: World Health Organization Shortened Quality of Life Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahar Barandaf

Imam Reza International University

bbarandaf@gmail.com+98 51 3502 2058

Outcome results

None listed

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