Trial · NCT07880366
The Effect of Lifestyle Program Women With PCOS
NCT07880366, Not applicable, Active not recruiting, Government College University Faisalabad
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of Lifestyle Program Women With PCOS. Trials, record NCT07880366. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07880366
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of Lifestyle Program Women With PCOS
- NCT number
- NCT07880366
- Status
- Active not recruiting
- Phases
- Not applicable
- Enrollment
- 30 participants, actual
- Lead sponsor
- Government College University Faisalabad
- Conditions
- Polycystic Ovary Syndrome
- Interventions
- Lifestyle Modification Program (LMP)
- First posted
- 2026-10-19
- Last updated
- 2026-10-19
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Perceived Stress | Baseline (pre-intervention) and immediately after completion of the 2-week intervention (post-intervention). | Perceived stress will be assessed using the Perceived Stress Scale (PSS-10-U). The total scale score will be calculated according to the instrument's scoring instructions. Changes in perceived stress will be evaluated by comparing baseline and post-intervention scores. |
| Primary | Health-Promoting Lifestyle Profile-II (HPLP-II). | Baseline (pre-intervention) and immediately after completion of the 2-week intervention (post-intervention). | Health-promoting lifestyle behaviors will be assessed using the Health-Promoting Lifestyle Profile II (HPLP-II). The total score will be calculated according to the instrument's scoring instructions. Changes in health-promoting lifestyle behaviors will be evaluated by comparing baseline and post-intervention scores. |
| Primary | Change in Healthy Eating Habits | Baseline (pre-intervention) and immediately after completion of the 2-week intervention (post-intervention). | Healthy eating habits will be assessed using the Brief Healthy Eating Habits Scale (BHEHS-6B). The total score will be calculated according to the instrument's scoring instructions. Changes in healthy eating habits will be evaluated by comparing baseline and post-intervention scores. |
| Primary | PCOS-Related Quality of Life | Baseline (pre-intervention) and immediately after completion of the 2-week intervention (post-intervention). | PCOS-related quality of life will be assessed using the 26-item PCOS Quality of Life Questionnaire (PCOSQ-26). The total score will be calculated according to the instrument's scoring instructions. Changes in PCOS-related quality of life will be evaluated by comparing baseline and post-intervention scores. |
| Secondary | Change in Body Mass Index (BMI) | Baseline (pre-intervention) and immediately after completion of the 2-week intervention (post-intervention). | Body mass index (BMI) will be calculated by dividing body weight in kilograms by the square of height in meters (BMI = weight in kg / height in m²). BMI will be assessed at baseline and post-intervention to evaluate changes following the lifestyle modification program. Weight and height will be combined to calculate a single BMI value, expressed in kg/m². |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07880366
GET https://conductscience.org/api/trials/v1/NCT07880366/registered