CClinicalTrials.gg
Not yet recruitingNCT06990009Updated Jun 3, 2025

The Effect of Physical Exercise After Childbirth

An interventional study of exercise in Postpartum, sponsored by ümran erciyes. Not yet recruiting. Open to female participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-06-03.

Sponsored by ümran erciyes · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 1 month ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
108
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Female
01

Study summary

Postpartum women are recommended to engage in physical activity including moderate intensity aerobic and strengthening exercises for at least 150 minutes within one week. The benefits of postpartum exercise include strengthening abdominal muscles, increasing energy, preventing postpartum depression, reducing stress, improving sleep quality and losing excess weight gained during pregnancy. However, activity levels of women who have given birth are reported to be very low, despite the great benefits of exercise on physical and mental health. In a meta-analysis, it was stated that exercise can be used for counseling and therapeutic purposes to improve postpartum quality of life and reduce fatigue.

Read the detailed description

Although studies evaluating sleep quality, quality of life and fatigue of postpartum women have been found in the literature, no study evaluating the effect of postpartum physical exercise in Turkey has been found yet. Accordingly, this study was planned to evaluate the effect of physical exercise on sleep quality, quality of life and fatigue in postpartum women.

02

Conditions studied

  • Postpartum

Keywords

  • exercise
  • quality of life
  • fatigue
  • sleep
  • postpartum
03

In context

Lead sponsor

This is the only study on the registry with ümran erciyes as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Be over 18 years of age
  • Be able to read and write in Turkish
  • Be in the 24th postpartum hour
  • Have had a vaginal delivery
  • Have had a single live birth -Have had a single live birth
  • Be primiparous
  • Have given birth at term -Have given birth at term
  • Accept to participate in the study
  • Have no musculoskeletal disorder preventing exercise
  • Have no chronic disorder preventing exercise
  • Using a smart phone

Exclusion criteria

Exclusion Criteria:

  • Having a regular exercise program
  • Having a baby in intensive care
  • Having a psychiatric treatment in the postpartum period
  • Being multiparous
  • Willing to voluntarily leave the study
  • Did not perform the exercises more than two days in a week
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
108 participants (estimated)

Study arms

  • Experimental
    exercise

    In line with the Puerperium and Newborn Care Guide, an exercise implementation protocol will be prepared by obtaining the opinion of a group of 10 experts on the appropriateness of the exercises and when they should be started. In this direction, a brochure and a video will be created for the participants to practice the exercises. A pilot study will be conducted in a group of 10 people on the use of the brochure and video, and the brochure and video will be finalized. Participants will be asked to do these exercises for 30 minutes a day, five days a week for eight weeks. A reminder message will be sent to the exercise group by the researchers to remind them of the exercises and provide motivation for eight weeks.

    Behavioral: exercise

  • No intervention
    control

    The control group will not receive any intervention and routine care will continue.

Interventions

  • Behavioralexercise

    In line with the Puerperium and Newborn Care Guide, an exercise implementation protocol will be prepared by obtaining the opinion of a group of 10 experts on the appropriateness of the exercises and when they should be started. In this direction, a brochure and a video will be created for the participants to practice the exercises. A pilot study will be conducted in a group of 10 people on the use of the brochure and video, and the brochure and video will be finalized. Participants will be asked to do these exercises for 30 minutes a day, five days a week for eight weeks. A reminder message will be sent to the exercise group by the researchers to remind them of the exercises and provide motivation for eight weeks.

06

What researchers measure

Primary outcomes

  1. Physical exercise increases sleep quality in postpartum women

    Physical exercise improves sleep quality in postpartum women. Participants will be asked to do these exercises for 30 minutes a day, five days a week and for eight weeks in accordance with the brochure and video prepared for the exercise. An evaluation will be made with Pittsburg Sleep Quality Index at the 24th hour and in the fourth week after birth. The final evaluation will be made at the end of the eighth week. Pittsburg Sleep Quality Index was developed by Buysse et al. in 1989. Turkish validity and reliability study was conducted by Ağargün et al. in 1996. It consists of a total of 24 questions, 19 of which are answered by the individual and five of which are answered by the relative/roommate. The 19 questions answered by the individual are included in the scoring. It consists of seven components that assess sleep duration, subjective sleep quality, sleep efficiency, sleep latency, the degree to which sleep interferes with daytime activities and the use of sleeping pills.

    Time frame: 8 week

  2. Physical exercise increases the quality of life in postpartum women

    The WHOQOL-BREF-TR will be evaluated at 24 hours and 4 weeks after delivery. The final evaluation will be made at the end of the 8th week. The effect of exercise on quality of life will be evaluated. WHOQOL-BREF-TR is a scale developed by the World Health Organization's Quality of Life Group to assess how people perceive their quality of life. The Turkish validity and reliability study of the questionnaire was conducted by Eser and colleagues in 1999. It is a shortened version of the 100-question quality of life scale reduced to 26 questions. The 27th question is a national question. While answering the questions, people are asked to think about the last 15 days of their lives. It is a five-point Likert-type scale. Scores are calculated in four domains and the first two questions are general health assessments and are not used to calculate quality of life.

    Time frame: 8 week

  3. Physical exercise reduces fatigue in postpartum women

    Participants will be asked to do the exercises for 30 minutes a day, five days a week, and for eight weeks. The Piper Fatigue Scale will be used to evaluate the 24th hour and fourth week after birth. The final evaluation will be made at the end of the eighth week. The effect of exercise on reducing fatigue will be evaluated. Piper Fatigue Scale: In 1998, it was developed by F. Piper and colleagues. Turkish validity and reliability study was conducted by Can et al. in 2001. It consists of 22 items and four sub-dimensions. When calculating the score, each item is scored between 0-10 and the total score is divided by the number of items. To calculate the subscale scores, the items in each subscale are summed and divided by the number of items in the relevant subscale. A high score on the scale indicates a high level of fatigue. While the total cronbach alpha coefficient of the scale is 0.94, the value of the subscales varies between 0.87-0.91.

    Time frame: 8 week

07

Study locations

No study locations are listed for this record.

08

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 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06990009
Lead sponsor
ümran erciyes
Collaborators
Istanbul University - Cerrahpasa
Responsible party
ümran erciyes (Master of Science, Istanbul University - Cerrahpasa) — Sponsor-investigator
First posted
May 25, 2025
Start date
Aug 15, 2025 (estimated)
Primary completion
Aug 15, 2025 (estimated)
Completion
Mar 30, 2026 (estimated)
Last update
Jun 3, 2025

Study contacts

Ümran ERCİYES
Contact
umranerciyes@gmail.com
+905432070138
Tülay YILMAZ
study director · Istanbul University - Cerrahpasa

Oversight

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

Not currently enrolling

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

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