Clinical trial · Interventional
Rehabilitation of Women Following Treatment for Gynaecological Cancer; a Randomized, Controlled Study
NCT01304745CI-TRIAL-00011245unknownPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of the study is to evaluate and compare the effect of: 1 Educational and counselling in groups, 2) Physical training in group with 3) Control group, on global- and health related quality of life and coping in patients finished treatment for gynaecological cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gynecologic Cancer | Malignant Female Reproductive System Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Educational and counseling in group | Behavioral | — | UNRESOLVED |
| Physical training in group | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Physical traning in group
- interventionNames
- Behavioral: Physical training in group
- type
- EXPERIMENTAL
- label
- Educational and counselling group
- interventionNames
- Behavioral: Educational and counseling in group
- type
- NO_INTERVENTION
- label
- Control group
Primary outcomes (1)
- measure
- Global- and health related quality of life
- timeFrame
- Pre intervention, post intervention and at one year follow-up
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Women finished treatment with a curative purpose independent of stage of cancer, type of gynaecological cancer, or previous gynaecological cancer * Meet a certain physical functioning criteria (Specified as; manage to walk 3.1 miles per hour, lie down and rise up from the floor) * To be willing to participate in the study for a period of 1- year and agrees to participate as specified conditions according to the consent form * Not having any significant amnesic symptoms * Women with other diagnosis were included as far as criterion 3 was fulfilled
References
Publications (0)
Data not yet available
No reference posted for this study.