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NCT Number: NCT07542600

Effect of Comprehensive Spa Rehabilitation on Female Infertility: A Clinical Study in Adult Women (Infertility-Spa)

This is a prospective, single-arm, pretest-posttest study evaluating the effects of a 21-day comprehensive spa treatment (Komplexní lázeňská léčebně rehabilitační péče, KLP) on female infertility at spa facility in Františkovy Lázně, Czech Republic.

The study enrolls 55 women aged 20-40 years diagnosed with infertility. The primary objective is to assess changes in hormonal profile before and after treatment.

Secondary objectives include evaluation of body composition, psychometric outcomes and long-term reproductive outcomes.

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Key information

Age range

20 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Spa Resort Pawlik-Aquaforum

Františkovy Lázně, Carlsbad Region, 35101, Czechia

Location status: Recruiting

Location contact

Edita Šimáčková

CONTACT

[email protected]

+420 724 163 127

About this study

STUDY DESIGN AND SETTING:

This is a prospective, single-arm interventional study using a one-group pretest-posttest design conducted at a spa facility in Františkovy Lázně, Czech Republic.

The study evaluates the effects of standard comprehensive spa treatment on women with infertility. The treatment is provided as part of routine clinical care covered by health insurance. The study does not modify the treatment protocol and only collects clinical data before and after treatment.

INTERVENTION:

The intervention is a standard 21-day comprehensive spa treatment program (KLP) based on natural healing resources of Františkovy Lázně.

The treatment includes:

  • peloid therapy (peat applications, vaginal tampons)
  • mineral water procedures (baths, vaginal irrigations)
  • carbon dioxide therapy
  • physiotherapy (including Mojžíšová method)
  • exercise therapy and rehabilitation
  • dietotherapy and lifestyle education Each patient undergoes a standardized spa treatment program prescribed individually by a physician.

ASSESSMENT SCHEDULE:

All assessments are performed at two time points:

  • baseline (no later than day 3 after admission)
  • end of treatment (day 19-21)

Measured parameters:

  • hormonal profile (LH, FSH, prolactin, estradiol, progesterone, testosterone, AMH)
  • ultrasound examination (folliculometry, endometrial thickness)[MV3.1]
  • physical examination
  • questionnaire-based assessments:
  • PSS-10 (Perceived Stress Scale)
  • EQ-5D-5L (quality of life)
  • FertiQoL
  • BAS 2

FOLLOW-UP:

Participants will be contacted at:

  • 6 months after treatment
  • 12 months after treatment

Collected data (questionnaire):

  • pregnancy occurrence
  • method of conception (spontaneous vs assisted reproduction)
  • pregnancy outcome (e.g., miscarriage, live birth) Participants may also be asked to complete follow-up questionnaires (PSS-10 and EQ-5D-5L), depending on feasibility.

DATA MANAGEMENT:

All patient data are pseudonymized using unique ID codes assigned at enrollment. Data are collected in both paper and electronic form. Paper records are stored in individual binders organized by patient ID. Data handling complies with EU General Data Protection Regulation (GDPR, Regulation 2016/679) and Good Clinical Practice principles. ILaB is responsible for the final statistical analysis and interpretation of the collected data.

ETHICAL CONSIDERATIONS:

The study was approved by the Ethics Committee of the University Hospital and Faculty of Medicine in Pilsen (reference no. 431/23, approved on November 2, 2023).

All participants provide written informed consent before enrollment. The study procedures represent minimal risk and correspond to standard clinical practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female, age 20-40 years
  • Diagnosis of infertility (primary or secondary)
  • History of at least one unsuccessful embryo transfer

Exclusion criteria

  • Contraindications to spa treatment
  • Acute gynecological inflammation
  • Severe comorbidities affecting study outcomes
  • Oncological disease
  • Alcohol intake >20 g/day
  • Non-compliance with treatment
  • Diagnosed with endometriosis

Treatment and study plan

Comrehensive Spa Treatment (KLP)

Procedure

A 21-day comprehensive spa treatment program including balneotherapy, peloid therapy, physiotherapy, and lifestyle interventions.

Primary outcomes

  1. Change in hormonal profile

    Time frame: Baseline to end of treatment (21 days)

    Change in serum levels of LH, FSH, prolactin, estradiol, progesterone, testosterone, and AMH between baseline and end of treatment.

Secondary outcomes

  1. Perceived stress (PSS-10)

    Time frame: Baseline (Day 1) and end of treatment (Day 21)

    Change in Perceived Stress Scale-10 total score (range 0 to 40; higher scores indicate greater perceived stress).

  2. Quality of life (EQ-5D-5L)

    Time frame: Baseline (Day 1) and end of treatment (Day 21)

    Change in EQ-5D-5L health-related quality of life index score and EQ Visual Analogue Scale score (VAS 0 to 100; higher scores indicate better perceived health).

  3. Pregnancy outcomes

    Time frame: Assessed at 6 months and 12 months after completion of treatment

    Occurrence of pregnancy, method of conception (natural conception or assisted reproduction), and pregnancy outcome (ongoing pregnancy, live birth, miscarriage).

  4. Body composition

    Time frame: Baseline (Day 1) and end of treatment (Day 21)

    Change in body composition parameters including body fat mass, skeletal muscle mass, fat-free mass, and total body water measured using bioelectrical impedance analysis (InBody).

Sponsors and collaborators

Lead sponsor

Institute of Spa and Balneology, public research institution

Other

Collaborators

  • Františkovy lázně

Registry information

Official study title

Objective Assessment of the Effect of Comprehensive Spa Rehabilitation Care on Female Infertility: A Prospective Interventional Clinical Study

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Apr 21, 2026
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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