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The effect of kinesio tape on low back pain and performance dysfunction in pregnant women

The effect of kinesio tape on low back pain and performance dysfunction in pregnant women presenting to comprehensive health centers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181210041911N1
Enrollment
80
Registered
2019-04-07
Start date
2019-01-18
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

Low back pain and Performance disability of the second and third trimester of pregnancy. Other specified pregnancy related conditions

Interventions

Intervention 1: The intervention group: Kinesio adhesive tape, 5-meter roll and 5 cm wide (made in Korea). two strips of 20 centimeters with a width of 5 centimeters are placed with medium stretching

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Written informed consent Age:18-40 years old Being pregnant in the second or third trimester (gestational age of 18-32 week) Mild to moderate low back pain (Visual analogue scale 1-7) No known or suspected orthopedic or rheumatologic disorders including scoliosis, spine injuries,rheumatoid arthritis No known intervertebral discopathy No skin lesion in the lumbosacral area No vertebral anomaly NO skin allergy Singleton pregnancy NO history of low back pain prior to pregnancy No addiction No NSAID consumption No history of other non-medical treatments

Exclusion criteria

Exclusion criteria: Allergy to kinesio tape kinesio tape coming off before the fifth day Any uncontrolled medical condition Severe low back pain (Visual analogue scale 7-10) Unwillingness to continue the study

Design outcomes

Primary

MeasureTime frame
Low back pain score with visual analogue scale(vas). Timepoint: Measurement of low back pain before intervention and 1?2?7 and 14 days after intervention. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Functional disability score with Roland morris disability questionnaire. Timepoint: Measurement of disability before intervention and 7?14 days after intervention. Method of measurement: Roland morris disability questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTayebeh alishahi

Rafsanjan University of Medical Sciences

www.alishahitayebeh@yahoo.com+98 34 3425 5900

Outcome results

None listed

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