NCT07683494

Brief Summary

Kinesiotape versus compression stockings on pregnant leg cramps and sleep quality

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
4mo left

Started Jul 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress29%
Jul 2026Dec 2026

First Submitted

Initial submission to the registry

June 19, 2026

Completed
12 days until next milestone

Study Start

First participant enrolled

July 1, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 6, 2026

Completed
26 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Expected
Last Updated

July 6, 2026

Status Verified

June 1, 2026

Enrollment Period

1 month

First QC Date

June 19, 2026

Last Update Submit

June 27, 2026

Conditions

Keywords

Leg cramps in pregnant womenKinesiotape

Outcome Measures

Primary Outcomes (2)

  • Muscle cramp characteristics measured using The Cramp Questionnaire

    Change in leg cramp frequency assessed using the Leg Cramp Questionnaire. Higher scores indicate greater cramp frequency.

    Baseline and after4weeks

  • Leg cramp pain intensty measured using visual analogue scale

    Pain intensity using visual analogue scale 0=no pain,10=wirst pain

    Baseline and after4weeks

Secondary Outcomes (2)

  • Sleep quality measured using sleep quality index

    Baseline and after4weeks

  • Quality of life measured using 12-item short form health survey

    Baseline and after4weeks

Study Arms (3)

Control

ACTIVE COMPARATOR

Control group receive instructions about dealing with leg cramps at bedtime

Other: Control group

Kinesiotape group

EXPERIMENTAL

Application of kinesiology tape to the lower leg muscles for 48 hours, applied twice a week for 4 weeks, in addition to standard instructions for managing leg cramps at bedtime

Other: Control groupOther: Kinesiotape group

Compression stockings group

EXPERIMENTAL

Use of graduated compression stockings worn daily for a period of 4 weeks, in addition to standard instructions for managing leg cramps at bedtime.

Other: Control groupOther: Compression stockings group

Interventions

Receive instructions about dealing with leg cramps at bedtime as sustained stretch,massage and optimal sleeping position

Compression stockings groupControlKinesiotape group

Application of kinesiology tape to the lower leg muscles for 48 hours, applied twice a week for 4 weeks, in addition to standard instructions for managing leg cramps at bedtime

Kinesiotape group

Use of graduated compression stockings worn daily for a period of 4 weeks, in addition to standard instructions for managing leg cramps at bedtime.

Compression stockings group

Eligibility Criteria

Age25 Weeks - 35 Weeks
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsAs the study targets leg cramps in pregnant women
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Pregnant female suffering from calf cramps. 2-Their ages range from 25to 35 years. 3-Their body mass index ranges from 25 to 29.9kg/m2. 4-Pregnant female in the second or third trimester.

You may not qualify if:

  • Skin abnormalities \[malignancy or burn in the treated area\]. 2-History of previous back surgery. 3-Present of any neuromuscular disease \[like multiple sclerosis\]. 4-Sensory disturbances. 5-Evidence of previous vertebral fractures or spinal structural abnormalities. 6-Women who have eclampsia or pre-eclampsia. 7-History of edema, thrombosis, venous thrombosis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Elnasria medical centre

Samannoud, Elgharbia, Egypt

Location

Elnasria medical centre

Samanonud, Elgharbia, Egypt

Location

MeSH Terms

Interventions

Control Groups

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Officials

  • Noha Fathy khalifa, Bachelor

    Faculty of physical therapy kafrelsheikh university

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Noha Fathy Khalifa, Bachelor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior of physical therapy at elnasria medical centre -samnoud

Study Record Dates

First Submitted

June 19, 2026

First Posted

July 6, 2026

Study Start

July 1, 2026

Primary Completion

August 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

July 6, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Individual participants data will not be shared

Locations