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Active, not recruitingNCT07036913Updated Jun 25, 2025

Effectiveness of ST With TENS and Stretching Exercises on Menstrual Pain and QOL With Dysmenorrhea. RCT

An interventional study of somatocognitive therapy and Stretching exercises in Dysmenorrhea, sponsored by Superior University. Active, not recruiting at 1 site in Pakistan. Open to female participants aged 13 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-06-25.

Sponsored by Superior University · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Mar 2025, registered Jun 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
13 Years to 45 Years
Sex
Female
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Study summary

Effectiveness of somatocognitive therapy with TENS and stretching exercises on menstrual pain and quality of life with dysmenorrhea.A randomized controlled trial The objective of this study is to find weather which therapy; somatocognitive therapy along with TENS or stretching exercises is more effective and what are their effects on quality of life in females with dysmonarrhea.

Read the detailed description

The Study spans the population into two groups. For first group we will give somatocognitive therapy (drawing and music) along with TENS and in second group we will give stretching exercises. In both groups the hotpack will be the common treatment.

The nature of this study will be randomized controlled trial . We will use simple random sampling technique in this study.

For outcomes measurements we will use numerical rating scale and menustral distress questionere .

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Conditions studied

  • Dysmenorrhea

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03

In context

Dysmenorrhea

398 studies on the registry are indexed under Dysmenorrhea; 96 are open to participants now.

This study's enrollment of 40 is below the median of 60 across 333 interventional studies indexed under Dysmenorrhea.

Browse Dysmenorrhea studies →

Lead sponsor

Superior University is the lead sponsor of 242 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
13 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Females who are facing menustral pain during their every menses.
  • Females who are facing dysmonarrhea from the at least last three months.
  • Females who are willing to take part in the research.

Exclusion criteria

Exclusion Criteria:

  • Females with some hormonal problem.
  • Females with irregular menustral cycle.
  • Females who face menustral pain during some of their menses
  • Pregnant females
  • Females with recent abdominal/pelvic surgery.
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    somatocognitive therapy

    Diagnostic Test: somatocognitive therapy

  • Active comparator
    Stretching exercises

    Combination Product: Stretching exercises

Interventions

  • Diagnostic testsomatocognitive therapy

    In somatocognitive therapy which includes drawing( three days prior to menustration in first two months and the first day of menustration in third month) and music(in the first 12 hours of menustration)along with TENS(thirty minutes on abdominal region, upon the onset of dysmonarrhea).

  • Combination productStretching exercises

    Stretching exercises of abdominal, lumbar or pelvic region will be performed as a treatment. Frequency:15 minutes;three times per week.

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What researchers measure

Primary outcomes

  1. Numerical rating scale

    A pain screening tool, commonly use to assess pain severity at that moment in time using a 0-10 scale, with 0 meaning "no pain" and 10 meaning "the worst pain".

    Time frame: 6 Month

  2. Menstrual distress questionnaire

    The MSQ is a 24-46 item self-report measure which assesses menstrual pain and symptoms .The score on each item ranges from 1 (never) to 5 (always) with a higher composite score indicating more symptoms.

    Time frame: 6 Months

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Study locations

1 site
  • Lahore City
    Lahore, Pakistan
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07036913
Lead sponsor
Superior University
Responsible party
Muhammad Naveed Babur (Principal Investigator, Superior University) — Principal investigator
First posted
Jun 25, 2025
Start date
Mar 4, 2025
Primary completion
Jun 1, 2025
Completion
Sep 30, 2025 (estimated)
Last update
Jun 25, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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